LYN
Normalized values from positional scanning peptide array
Phospho-serine (pS) is a duplicate of phospho-tyrosine (pT) in PSPA
Position-wise Probabilities
Log-Odds: Probabilities / STY Background
Sites with acceptor types representing >8% and count ≥10 are included
Y Sites Probabilities
Log-Odds: Y Sites / Y Background
Sites with acceptor types representing >8% and count ≥10 are included
Motif clusters with count ≥ 10 are shown
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| substrate_uniprot | site | source | substrate_genes | site_seq |
|---|---|---|---|---|
| A0MZ66 | Y24 | Sugiyama | SHTN1 KIAA1598 | sDEEKQLQLITsLKEQAIGEyEDLRAENQKTKEKCDKIRQE |
| A1L429 | Y10 | Sugiyama | GAGE12B; GAGE12C; GAGE12D; GAGE12E | ___________MSWRGRsTyyWPRPRRYVQPPEMIGPMRPE |
| A1L429 | Y9 | Sugiyama | GAGE12B; GAGE12C; GAGE12D; GAGE12E | ____________MSWRGRsTyyWPRPRRYVQPPEMIGPMRP |
| A5A3E0 | S939 | Sugiyama | POTEF A26C1B | VALDFEQEMATVAsSSSLEKsyELPDGQVItIGNERFRCPE |
| A5A3E0 | Y1062 | Sugiyama | POTEF A26C1B | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCL_______ |
| A5A3E0 | Y791 | Sugiyama | POTEF A26C1B | MEHGIITNWDDMEKIWHHtFyNELRVAPEEHPVLLTEATLN |
| A5A3E0 | Y940 | Sugiyama | POTEF A26C1B | ALDFEQEMATVAsSSSLEKsyELPDGQVItIGNERFRCPEA |
| A5YKK6 | Y851 | Sugiyama | CNOT1 CDC39 KIAA1007 NOT1 AD-005 | QVWPEANQHFSKEIDDEANSyFQRIYNHPPHPTMSVDEVLE |
| A6NDE8 | Y10 | Sugiyama | GAGE12H | ___________MSWRGRsTyyWPRPRRYVQPPEMIGPMRPE |
| A6NDE8 | Y9 | Sugiyama | GAGE12H | ____________MSWRGRsTyyWPRPRRYVQPPEMIGPMRP |
| A6NER3 | Y10 | Sugiyama | GAGE12J | ___________MSWRGRsTyyWPRPRPYVQPPEMIGPMRPE |
| A6NER3 | Y9 | Sugiyama | GAGE12J | ____________MSWRGRsTyyWPRPRPYVQPPEMIGPMRP |
| A6NMY6 | Y147 | Sugiyama | ANXA2P2 ANX2L2 ANX2P2 LPC2B | sLIEIICsRtNQELQEINRVyKEMYKtDLEKDIIsDtsGDF |
| A6NMY6 | Y333 | Sugiyama | ANXA2P2 ANX2L2 ANX2P2 LPC2B | KsLyyyIQQDTKGDyQKALLyLCGGDD______________ |
| O00116 | Y645 | Sugiyama | AGPS AAG5 | QWLKESIsDVGFGMLKSVKEyVDPNNIFGNRNLL_______ |
| O00170 | Y202 | Sugiyama | AIP XAP2 | IHQEGNRLYREGHVKEAAAKyyDAIACLKNLQMKEQPGSPE |
| O00170 | Y203 | Sugiyama | AIP XAP2 | HQEGNRLYREGHVKEAAAKyyDAIACLKNLQMKEQPGSPEW |
| O00193 | Y84 | Sugiyama | SMAP C11orf58 | TSHFRTGEEDKKINEELEsQyQQsMDsKLSGRYRRHCGLGF |
| O00232 | Y20 | Sugiyama | PSMD12 | _MADGGSERADGRIVKMEVDysATVDQRLPECAKLAKEGRL |
| O00233 | Y41 | Sugiyama | PSMD9 | SDVQELMRRKEEIEAQIKANyDVLEsQKGIGMNEPLVDCEG |
| O00233 | Y70 | Sugiyama | PSMD9 | IGMNEPLVDCEGyPRSDVDLyQVRTARHNIICLQNDHKAVM |
| O00264 | Y113 | Sugiyama | PGRMC1 HPR6.6 PGRMC | INGKVFDVTKGRKFyGPEGPyGVFAGRDASRGLATFCLDKE |
| O00299 | Y233 | Sugiyama | CLIC1 G6 NCC27 | AyAREEFAstCPDDEEIELAyEQVAKALK____________ |
| O00401 | Y256 | Sugiyama | WASL | FDMCGIsEAQLKDRETSKVIyDFIEKTGGVEAVKNELRRQA |
| O00410 | Y33 | Sugiyama | IPO5 KPNB3 RANBP5 | LLLGNLLsPDNVVRKQAEEtyENIPGQSKITFLLQAIRNTT |
| O00469 | Y444 | Sugiyama | PLOD2 | LWSNFWGALSPDGYYARsEDyVDIVQGNRVGVWNVPYMANV |
| O00469 | Y586 | Sugiyama | PLOD2 | FWFPIFSEKACDELVEEMEHyGKWSGGKHHDsRIsGGyENV |
| O00488 | Y97 | Sugiyama | ZNF593 ZT86 | KTHFRSKDHKKRLKQLsVEPysQEEAERAAGMGSYVPPRRL |
| O00625 | Y131 | Sugiyama | PIR | AHGLQLWVNLRSSEKMVEPQyQELKSEEIPKPSKDGVTVAV |
| O14579 | Y304 | Sugiyama | COPE | HPFIKEYQAKENDFDRLVLQyAPsA________________ |
| O14602 | Y106 | Sugiyama | EIF1AY | DNKADVILKYNADEARsLKAyGELPEHAKINETDTFGPGDD |
| O14818 | T147 | Sugiyama | PSMA7 HSPC | FGISALIVGFDFDGTPRLyQtDPsGtyHAWKANAIGRGAKS |
| O14818 | Y153 | Sugiyama | PSMA7 HSPC | IVGFDFDGTPRLyQtDPsGtyHAWKANAIGRGAKSVREFLE |
| O14818 | Y176 | Sugiyama | PSMA7 HSPC | WKANAIGRGAKSVREFLEKNyTDEAIETDDLTIKLVIKALL |
| O14910 | S130 | Sugiyama | LIN7A MALS1 VELI1 | ELPKTDEGLGFNVMGGKEQNsPIyIsRIIPGGVAERHGGLK |
| O14910 | Y133 | Sugiyama | LIN7A MALS1 VELI1 | KTDEGLGFNVMGGKEQNsPIyIsRIIPGGVAERHGGLKRGD |
| O14920 | Y188 | EPSD|PSP | IKBKB IKKB | GYAKELDQGsLCTsFVGTLQyLAPELLEQQKyTVTVDYWSF |
| O14920 | Y199 | EPSD|PSP | IKBKB IKKB | CTsFVGTLQyLAPELLEQQKyTVTVDYWSFGTLAFECITGF |
| O14950 | Y143 | Sugiyama | MYL12B MRLC2 MYLC2B | LRELLttMGDRFtDEEVDELyREAPIDKKGNFNyIEFtRIL |
| O14950 | Y156 | Sugiyama | MYL12B MRLC2 MYLC2B | DEEVDELyREAPIDKKGNFNyIEFtRILKHGAKDKDD____ |
| O14974 | Y911 | Sugiyama | PPP1R12A MBS MYPT1 | ETssTsAGDRyDsLLGRsGsysYLEERKPYSSRLEKDDSTD |
| O14979 | Y167 | Sugiyama | HNRNPDL HNRPDL JKTBP | DGKMFIGGLSWDTsKKDLtEyLSRFGEVVDCtIKTDPVTGR |
| O15013 | Y1307 | Sugiyama | ARHGEF10 KIAA0294 | sLsLsHGsssLEHRSEDsTIyDLLKDPVSLRSKARRAKKAK |
| O15067 | Y538 | Sugiyama | PFAS KIAA0361 | GAGGNGNVLKELsDPAGAIIytsRFQLGDPTLNALEIWGAE |
| O15230 | Y81 | Sugiyama | LAMA5 KIAA0533 KIAA1907 | SATCGEEAPARGSPRPTEDLyCKLVGGPVAGGDPNQTIRGQ |
| O15357 | Y1135 | Sugiyama | INPPL1 SHIP2 | SGDDRSCSVLQMAKTLSEVDyAPAGPARSALLPGPLELQPP |
| O15357 | Y190 | Sugiyama | INPPL1 SHIP2 | AAESAPNGLSTVSHDYLKGsyGLDLEAVRGGASHLPHLTRT |
| O15371 | Y30 | Sugiyama | EIF3D EIF3S7 | QDNPSGWGPCAVPEQFRDMPyQPFsKGDRLGKVADWtGAty |
| O15371 | Y50 | Sugiyama | EIF3D EIF3S7 | yQPFsKGDRLGKVADWtGAtyQDKRYTNKYSSQFGGGSQYA |
| O15372 | Y350 | Sugiyama | EIF3H EIF3S3 | IKEFTAQNLGKLFMAQALQEyNN__________________ |
| O15492 | Y168 | SIGNOR|iPTMNet|EPSD|PSP | RGS16 RGSR | TATCFDAAQGKTRTLMEKDSyPRFLKSPAyRDLAAQASAAS |
| O15492 | Y177 | GPS6|ELM|iPTMNet|EPSD|PSP | RGS16 RGSR | GKTRTLMEKDSyPRFLKSPAyRDLAAQASAASATLSSCsLD |
| O15524 | Y80 | SIGNOR|PSP | SOCS1 SSI1 TIP3 | SHADYRRITRASALLDACGFyWGPLSVHGAHERLRAEPVGT |
| O43172 | Y31 | Sugiyama | PRPF4 PRP4 | ATKTKAPDDLVAPVVKKPHIyyGsLEEKERERLAKGESGIL |
| O43172 | Y32 | Sugiyama | PRPF4 PRP4 | TKTKAPDDLVAPVVKKPHIyyGsLEEKERERLAKGESGILG |
| O43252 | Y617 | Sugiyama | PAPSS1 ATPSK1 PAPSS | EGQKPPEGFMAPKAWtVLtEyyKSLEKA_____________ |
| O43252 | Y618 | Sugiyama | PAPSS1 ATPSK1 PAPSS | GQKPPEGFMAPKAWtVLtEyyKSLEKA______________ |
| O43390 | Y376 | Sugiyama | HNRNPR HNRPR | ILEKSFSEFGKLERVKKLKDyAFVHFEDRGAAVKAMDEMNG |
| O43448 | Y311 | Sugiyama | KCNAB3 KCNA3B | LITSKYDGRVPDTCRASIKGyQWLKDKVQSEDGKKQQAKVM |
| O43684 | Y141 | Sugiyama | BUB3 | KLWDPRtPCNAGTFsQPEKVytLSVSGDRLIVGTAGRRVLV |
| O43707 | Y234 | Sugiyama | ACTN4 | KLRKDDPVTNLNNAFEVAEKyLDIPKMLDAEDIVNtARPDE |
| O43707 | Y397 | Sugiyama | ACTN4 | GKMVSDINNGWQHLEQAEKGyEEWLLNEIRRLERLDHLAEK |
| O43707 | Y441 | Sugiyama | ACTN4 | KAsIHEAWtDGKEAMLKHRDyEtAtLsDIKALIRKHEAFEs |
| O43707 | Y878 | Sugiyama | ACTN4 | DKNFITAEELRRELPPDQAEyCIARMAPyQGPDAVPGALDy |
| O43707 | Y886 | Sugiyama | ACTN4 | ELRRELPPDQAEyCIARMAPyQGPDAVPGALDyKsFStALy |
| O43707 | Y898 | Sugiyama | ACTN4 | yCIARMAPyQGPDAVPGALDyKsFStALyGEsDL_______ |
| O43707 | Y906 | Sugiyama | ACTN4 | yQGPDAVPGALDyKsFStALyGEsDL_______________ |
| O43765 | Y158 | Sugiyama | SGTA SGT SGT1 | LGNyAGAVQDCERAICIDPAySKAYGRMGLALSSLNKHVEA |
| O43765 | Y195 | Sugiyama | SGTA SGT SGT1 | HVEAVAYYKKALELDPDNEtyKsNLKIAELKLREAPSPTGG |
| O43823 | Y146 | EPSD|PSP | AKAP8 AKAP95 | FRFQPFESYDSRPCLPEHNPyRPSySyDyEFDLGSDRNGsF |
| O43823 | Y150 | EPSD|PSP | AKAP8 AKAP95 | PFESYDSRPCLPEHNPyRPSySyDyEFDLGSDRNGsFGGQy |
| O43823 | Y152 | EPSD|PSP | AKAP8 AKAP95 | ESYDSRPCLPEHNPyRPSySyDyEFDLGSDRNGsFGGQySE |
| O43823 | Y154 | EPSD|PSP | AKAP8 AKAP95 | YDSRPCLPEHNPyRPSySyDyEFDLGSDRNGsFGGQySECR |
| O43823 | Y170 | EPSD|PSP | AKAP8 AKAP95 | ySyDyEFDLGSDRNGsFGGQySECRDPARERGSLDGFMRGR |
| O43823 | Y311 | EPSD|PSP | AKAP8 AKAP95 | RGFDRFGPDGTGRKRKQFQLyEEPDtKLARVDsEGDFsEND |
| O43823 | Y436 | EPSD|PSP | AKAP8 AKAP95 | ETLRFISTKLPDKTVEFLQEyIVNRNKKIEKRRQELMEKET |
| O43823 | Y51 | EPSD|PSP | AKAP8 AKAP95 | GYENYNYYGAQNTSVTTGATySyGPASWEAAKANDGGLAAG |
| O43823 | Y53 | EPSD|PSP | AKAP8 AKAP95 | ENYNYYGAQNTSVTTGATySyGPASWEAAKANDGGLAAGAP |
| O43823 | Y539 | EPSD|PSP | AKAP8 AKAP95 | SLHVAKSVLNNRHIVKMLEKyLKGEDPFTSETVDPEMEGDD |
| O43823 | Y80 | EPSD|PSP | AKAP8 AKAP95 | AAKANDGGLAAGAPAMHMASyGPEPCTDNSDsLIAKINQRL |
| O43852 | Y106 | Sugiyama | CALU | GFVtVDELKDWIKFAQKRWIyEDVERQWKGHDLNEDGLVsW |
| O43852 | Y185 | Sugiyama | CALU | KDGDLIATKEEFtAFLHPEEyDyMKDIVVQEtMEDIDKNAD |
| O43852 | Y263 | Sugiyama | CALU | KNRDGKMDKEEtKDWILPsDyDHAEAEARHLVyEsDQNKDG |
| O43852 | Y47 | Sugiyama | CALU | RVHHEPQLsDKVHNDAQsFDyDHDAFLGAEEAKtFDQLtPE |
| O60264 | Y80 | Sugiyama | SMARCA5 SNF2H WCRF135 | EIFDDAsPGKQKEIQEPDPtyEEKMQTDRANRFEYLLKQTE |
| O60361 | Y136 | Sugiyama | NME2P1 | SLRFKPEELVDYKSCAHDWVyE___________________ |
| O60496 | Y271 | iPTMNet|EPSD | DOK2 | ATPQPQPATIPASLPRPDsPySRPHDsLPPPsPTTPVPAPR |
| O60496 | Y299 | iPTMNet|EPSD | DOK2 | PPPsPTTPVPAPRPRGQEGEyAVPFDAVARSLGKNFRGILA |
| O60496 | Y345 | iPTMNet|EPSD | DOK2 | LADPLYDSIEETLPPRPDHIyDEPEGVAALSLYDSPQEPRG |
| O60664 | Y95 | Sugiyama | PLIN3 M6PRBP1 TIP47 | VsGAQPILSKLEPQIAsAsEyAHRGLDKLEENLPILQQPTE |
| O60711 | Y72 | GPS6|SIGNOR|EPSD | LPXN LDLP | NTSPLPAQLVyTTNIQELNVySEAQEPKESPPPSKTSAAAQ |
| O60716 | Y228 | Sugiyama | CTNND1 KIAA0384 | yPPDGysRHyEDGyPGGsDNyGsLsRVtRIEERyRPsMEGy |
| O60739 | Y30 | Sugiyama | EIF1B | FDPFADATKGDDLLPAGTEDyIHIRIQQRNGRKtLttVQGI |
| O60814 | Y41 | Sugiyama | H2BC12 H2BFT HIRIP1 HIST1H2BK | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| O60814 | Y43 | Sugiyama | H2BC12 H2BFT HIRIP1 HIST1H2BK | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| O60841 | Y134 | Sugiyama | EIF5B IF2 KIAA0741 | EELEDKDsKSKKTAKPKVEMysGsDDDDDFNKLPKKAKGKA |
| O60869 | Y109 | Sugiyama | EDF1 | GLtQKDLATKINEKPQVIADyESGRAIPNNQVLGKIERAIG |
| O60884 | Y128 | Sugiyama | DNAJA2 CPR3 HIRIP4 | NGRRRGEDMMHPLKVsLEDLyNGKTTKLQLSKNVLCsACsG |
| O60884 | Y66 | Sugiyama | DNAJA2 CPR3 HIRIP4 | KFKEISFAyEVLSNPEKRELyDRyGEQGLREGsGGGGGMDD |
| O60884 | Y69 | Sugiyama | DNAJA2 CPR3 HIRIP4 | EISFAyEVLSNPEKRELyDRyGEQGLREGsGGGGGMDDIFS |
| O60927 | Y64 | Sugiyama | PPP1R11 HCGV TCTE5 | TsDTVDNEHMGRRssKCCCIyEKPRAFGEsstEsDEEEEEG |
| O75116 | Y936 | Sugiyama | ROCK2 KIAA0619 | EITLTKADSEQLARsIAEEQysDLEKEKIMKELEIKEMMAR |
| O75190 | Y4 | Sugiyama | DNAJB6 HSJ2 MRJ MSJ1 | _________________MVDyyEVLGVQRHAsPEDIKKAYR |
| O75190 | Y5 | Sugiyama | DNAJB6 HSJ2 MRJ MSJ1 | ________________MVDyyEVLGVQRHAsPEDIKKAYRK |
| O75223 | Y156 | Sugiyama | GGCT C7orf24 CRF21 | sPQYKKIICMGAKENGLPLEyQEKLKAIEPNDytGKVsEEI |
| O75347 | Y75 | Sugiyama | TBCA | EILQEsRMMIPDCQRRLEAAyLDLQRILENEKDLEEAEEyK |
| O75348 | Y47 | Sugiyama | ATP6V1G1 ATP6G ATP6G1 ATP6J | KRKNRRLKQAKEEAQAEIEQyRLQREKEFKAKEAAALGsRG |
| O75369 | T1575 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | QITDQEGKPKRAIVHDNKDGtyAVtyIPDKtGRYMIGVTYG |
| O75369 | Y2276 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | EPGNYEVSIKFNDEHIPEsPyLVPVIAPSDDARRLTVMSLQ |
| O75369 | Y902 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | VQFNsPLPGDAVKDLDIIDNyDysHtVKYtPtQQGNMQVLV |
| O75369 | Y904 | Sugiyama | FLNB FLN1L FLN3 TABP TAP | FNsPLPGDAVKDLDIIDNyDysHtVKYtPtQQGNMQVLVTY |
| O75534 | Y597 | Sugiyama | CSDE1 D1S155E KIAA0885 NRU UNR | EKVNKtHsVNGItEEADPTIysGKVIRPLRSVDPTQTEYQG |
| O75976 | Y1376 | Sugiyama | CPD | KKsLLsHEFQDEtDtEEEtLyssKH________________ |
| O76087 | Y10 | Sugiyama | GAGE7 GAGE12I GAGE7B | ___________MSWRGRsTyyWPRPRRYVQPPEMIGPMRPE |
| O76087 | Y9 | Sugiyama | GAGE7 GAGE12I GAGE7B | ____________MSWRGRsTyyWPRPRRYVQPPEMIGPMRP |
| O94842 | Y591 | Sugiyama | TOX4 C14orf92 KIAA0737 | RCVRsGCENPPIVSKDWDNEyCSNECVVKHCRDVFLAWVAS |
| O94906 | Y105 | Sugiyama | PRPF6 C20orf14 | AGSLFSSGPYEKDDEEADAIyAALDKRMDERRKERREQREK |
| O95218 | Y167 | Sugiyama | ZRANB2 ZIS ZNF265 | EVEDKEsEGEEEDEDEDLsKyKLDEDEDEDDADLsKyNLDA |
| O95297 | Y263 | Sugiyama | MPZL1 PZR UNQ849/PRO1787 | QLDHsGGHHSDKINKSEsVVyADIRKN______________ |
| O95336 | Y92 | Sugiyama | PGLS | RWtLGFCDERLVPFDHAEStyGLyRTHLLSRLPIPESQVIT |
| O95336 | Y95 | Sugiyama | PGLS | LGFCDERLVPFDHAEStyGLyRTHLLSRLPIPESQVITINP |
| O95347 | Y938 | Sugiyama | SMC2 CAPE SMC2L1 PRO0324 | SKHKREAEDGAAKVSKMLKDyDWINAERHLFGQPNSAYDFK |
| O95359 | Y2527 | Sugiyama | TACC2 | ETKFssPtEELDyRNsYEIEyMEKIGssLPQDDDAPKKQAL |
| O95433 | Y322 | Sugiyama | AHSA1 C14orf3 HSPC322 | MEGRGIPAPEEERTRQGWQRyyFEGIKQTFGYGARLF____ |
| O95433 | Y323 | Sugiyama | AHSA1 C14orf3 HSPC322 | EGRGIPAPEEERTRQGWQRyyFEGIKQTFGYGARLF_____ |
| O95757 | S599 | Sugiyama | HSPA4L APG1 HSPH3 OSP94 | sIDLPIQssLCRQLGQDLLNsyIENEGKMIMQDKLEKERND |
| O95757 | Y30 | Sugiyama | HSPA4L APG1 HSPH3 OSP94 | FLNCYIAVARsGGIETIANEySDRCtPACIsLGSRTRAIGN |
| O95757 | Y627 | Sugiyama | HSPA4L APG1 HSPH3 OSP94 | MIMQDKLEKERNDAKNAVEEyVyDFRDRLGtVYEKFITPED |
| O95757 | Y629 | Sugiyama | HSPA4L APG1 HSPH3 OSP94 | MQDKLEKERNDAKNAVEEyVyDFRDRLGtVYEKFITPEDLS |
| O95817 | T242 | Sugiyama | BAG3 BIS | QPsFHQAQKTHyPAQQGEyQtHQPVyHKIQGDDWEPRPLRA |
| O95817 | Y247 | Sugiyama | BAG3 BIS | QAQKTHyPAQQGEyQtHQPVyHKIQGDDWEPRPLRAAsPFR |
| P00338 | Y10 | Sugiyama | LDHA PIG19 | ___________MAtLKDQLIyNLLKEEQtPQNKITVVGVGA |
| P00338 | Y239 | Sugiyama | LDHA PIG19 | GtDKDKEQWKEVHKQVVEsAyEVIKLKGYtSWAIGLSVADL |
| P00390 | Y371 | Sugiyama | GSR GLUR GRD1 | TDDKGHIIVDEFQNtNVKGIyAVGDVCGKALLtPVAIAAGR |
| P00491 | Y166 | Sugiyama | PNP NP | PLRGPNDERFGDRFPAMsDAyDRtMRQRALstWKQMGEQRE |
| P00505 | Y96 | Sugiyama | GOT2 KYAT4 | VLPSVRKAEAQIAAKNLDKEyLPIGGLAEFCKASAELALGE |
| P00519 | Y115 | EPSD|PSP | ABL1 ABL JTK7 | HNGEWCEAQTKNGQGWVPSNyITPVNSLEKHSWyHGPVSRN |
| P00519 | Y128 | EPSD|PSP | ABL1 ABL JTK7 | QGWVPSNyITPVNSLEKHSWyHGPVSRNAAEyLLSSGINGS |
| P00519 | Y139 | EPSD|PSP | ABL1 ABL JTK7 | VNSLEKHSWyHGPVSRNAAEyLLSSGINGSFLVRESESSPG |
| P00519 | Y172 | EPSD|PSP | ABL1 ABL JTK7 | RESESSPGQRSISLRYEGRVyHYRINtASDGKLyVSSESRF |
| P00519 | Y185 | EPSD|PSP | ABL1 ABL JTK7 | LRYEGRVyHYRINtASDGKLyVSSESRFNTLAELVHHHSTV |
| P00519 | Y215 | EPSD|PSP | ABL1 ABL JTK7 | LAELVHHHSTVADGLITTLHyPAPKRNKPTVyGVSPNyDKW |
| P00519 | Y226 | EPSD|PSP | ABL1 ABL JTK7 | ADGLITTLHyPAPKRNKPTVyGVSPNyDKWEMERTDITMKH |
| P00519 | Y393 | EPSD|PSP | ABL1 ABL JTK7 | ENHLVKVADFGLSRLMtGDtytAHAGAKFPIKWTAPESLAy |
| P00519 | Y70 | EPSD|PSP | ABL1 ABL JTK7 | SKENLLAGPsENDPNLFVALyDFVAsGDNTLSITKGEKLRV |
| P00558 | Y161 | Sugiyama | PGK1 PGKA MIG10 OK/SW-cl.110 | KAEPAKIEAFRAsLSKLGDVyVNDAFGtAHRAHssMVGVNL |
| P00558 | Y76 | Sugiyama | PGK1 PGKA MIG10 OK/SW-cl.110 | KSVVLMSHLGRPDGVPMPDKysLEPVAVELKSLLGKDVLFL |
| P00966 | Y163 | Sugiyama | ASS1 ASS | APWRMPEFYNRFKGRNDLMEyAKQHGIPIPVtPKNPWSMDE |
| P02730 | Y21 | GPS6|ELM|iPTMNet|EPSD|PSP | SLC4A1 AE1 DI EPB3 | MEELQDDyEDMMEENLEQEEyEDPDIPEsQMEEPAAHDtEA |
| P02730 | Y359 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | SLC4A1 AE1 DI EPB3 | QRELLRRRYQssPAKPDssFyKGLDLNGGPDDPLQQTGQLF |
| P02730 | Y8 | GPS6|ELM|iPTMNet|EPSD|PSP | SLC4A1 AE1 DI EPB3 | _____________MEELQDDyEDMMEENLEQEEyEDPDIPE |
| P02730 | Y904 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | SLC4A1 AE1 DI EPB3 | QCLDADDAKAtFDEEEGRDEyDEVAMPV_____________ |
| P02786 | Y152 | Sugiyama | TFRC | sEKLDstDFTGtIKLLNENsyVPREAGsQKDENLALyVENQ |
| P02786 | Y402 | Sugiyama | TFRC | KEIKILNIFGVIKGFVEPDHyVVVGAQRDAWGPGAAKSGVG |
| P04075 | S346 | Sugiyama | ALDOA ALDA | EEYVKRALANsLACQGKytPsGQAGAAAsEsLFVsNHAy__ |
| P04075 | Y343 | Sugiyama | ALDOA ALDA | AAQEEYVKRALANsLACQGKytPsGQAGAAAsEsLFVsNHA |
| P04075 | Y364 | Sugiyama | ALDOA ALDA | tPsGQAGAAAsEsLFVsNHAy____________________ |
| P04080 | Y97 | Sugiyama | CSTB CST6 STFB | NKPLtLsNyQTNKAKHDELtyF___________________ |
| P04181 | Y50 | Sugiyama | OAT | TKKtVQGPPtSDDIFEREyKyGAHNyHPLPVALERGKGIyL |
| P04181 | Y55 | Sugiyama | OAT | QGPPtSDDIFEREyKyGAHNyHPLPVALERGKGIyLWDVEG |
| P04406 | Y314 | Sugiyama | GAPDH GAPD CDABP0047 OK/SW-cl.12 | tFDAGAGIALNDHFVKLIsWyDNEFGysNRVVDLMAHMAsK |
| P04406 | Y320 | Sugiyama | GAPDH GAPD CDABP0047 OK/SW-cl.12 | GIALNDHFVKLIsWyDNEFGysNRVVDLMAHMAsKE_____ |
| P04632 | Y87 | Sugiyama | CAPNS1 CAPN4 CAPNS | sAISEAAAQYNPEPPPPRtHysNIEANEsEEVRQFRRLFAQ |
| P04792 | S82 | Sugiyama | HSPB1 HSP27 HSP28 | AIEsPAVAAPAYsRALsRQLssGVsEIRHtADRWRVsLDVN |
| P04818 | Y135 | Sugiyama | TYMS TS OK/SW-cl.29 | RDFLDsLGFsTREEGDLGPVyGFQWRHFGAEyRDMEsDysG |
| P04843 | Y387 | Sugiyama | RPN1 | SLTVKIILPEGAKNIEIDsPyEISRAPDELHYTYLDTFGRP |
| P05187 | Y182 | Sugiyama | ALPP PLAP | GKSVGVVTTTRVQHAsPAGtyAHtVNRNWysDADVPASARQ |
| P05362 | T454 | Sugiyama | ICAM1 | DGtFPLPIGEsVtVtRDLEGtyLCRARSTQGEVTRKVTVNV |
| P05362 | Y455 | Sugiyama | ICAM1 | GtFPLPIGEsVtVtRDLEGtyLCRARSTQGEVTRKVTVNVL |
| P05455 | Y104 | Sugiyama | SSB | EDKTKIRRsPsKPLPEVTDEyKNDVKNRsVYIKGFPtDAtL |
| P05787 | S280 | Sugiyama | KRT8 CYK8 | IAEVKAQyEDIANRsRAEAEsMyQIKyEELQsLAGKHGDDL |
| P05787 | Y204 | Sugiyama | KRT8 CYK8 | NKRTEMENEFVLIKKDVDEAyMNKVELESRLEGLTDEINFL |
| P05787 | Y282 | Sugiyama | KRT8 CYK8 | EVKAQyEDIANRsRAEAEsMyQIKyEELQsLAGKHGDDLRR |
| P05787 | Y286 | Sugiyama | KRT8 CYK8 | QyEDIANRsRAEAEsMyQIKyEELQsLAGKHGDDLRRTKTE |
| P06493 | Y15 | EPSD|Sugiyama | CDK1 CDC2 CDC28A CDKN1 P34CDC2 | ______MEDyTKIEKIGEGtyGVVyKGRHKTTGQVVAMKKI |
| P06493 | Y19 | Sugiyama | CDK1 CDC2 CDC28A CDKN1 P34CDC2 | __MEDyTKIEKIGEGtyGVVyKGRHKTTGQVVAMKKIRLEs |
| P06733 | S268 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | ASEFFRsGKyDLDFKsPDDPsRyIsPDQLADLyKsFIKDyP |
| P06733 | S272 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | FRsGKyDLDFKsPDDPsRyIsPDQLADLyKsFIKDyPVVsI |
| P06733 | Y189 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | MILPVGAANFREAMRIGAEVyHNLKNVIKEKyGKDAtNVGD |
| P06733 | Y257 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | TDKVVIGMDVAASEFFRsGKyDLDFKsPDDPsRyIsPDQLA |
| P06733 | Y270 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | EFFRsGKyDLDFKsPDDPsRyIsPDQLADLyKsFIKDyPVV |
| P06733 | Y280 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | DFKsPDDPsRyIsPDQLADLyKsFIKDyPVVsIEDPFDQDD |
| P06733 | Y407 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | GLCtGQIKTGAPCRSERLAKyNQLLRIEEELGsKAKFAGRN |
| P06733 | Y44 | Sugiyama | ENO1 ENO1L1 MBPB1 MPB1 | LFtsKGLFRAAVPsGAstGIyEALELRDNDKtRYMGKGVSK |
| P06737 | Y778 | Sugiyama | PYGL | LFKDIINMLFYHDRFKVFADyEAyVKCQDKVSQLyMNPKAW |
| P06737 | Y781 | Sugiyama | PYGL | DIINMLFYHDRFKVFADyEAyVKCQDKVSQLyMNPKAWNTM |
| P06899 | Y41 | Sugiyama | H2BC11 H2BFR HIST1H2BJ | KAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P06899 | Y43 | Sugiyama | H2BC11 H2BFR HIST1H2BJ | QKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMGIM |
| P07195 | Y240 | Sugiyama | LDHB | GTDNDSENWKEVHKMVVEsAyEVIKLKGYTNWAIGLSVADL |
| P07195 | Y84 | Sugiyama | LDHB | MDLQHGsLFLQtPKIVADKDysVtANSKIVVVtAGVRQQEG |
| P07205 | Y161 | Sugiyama | PGK2 PGKB | KAEPDKIEAFRAsLSKLGDVyVNDAFGtAHRAHSSMVGVNL |
| P07237 | Y327 | Sugiyama | P4HB ERBA2L PDI PDIA1 PO4DB | LKKEECPAVRLITLEEEMTKyKPEsEELtAERItEFCHRFL |
| P07237 | Y94 | Sugiyama | P4HB ERBA2L PDI PDIA1 PO4DB | GSEIRLAKVDAtEEsDLAQQyGVRGyPtIKFFRNGDTASPK |
| P07237 | Y99 | Sugiyama | P4HB ERBA2L PDI PDIA1 PO4DB | LAKVDAtEEsDLAQQyGVRGyPtIKFFRNGDTASPKEytAG |
| P07355 | Y147 | Sugiyama | ANXA2 ANX2 ANX2L4 CAL1H LPC2D | sLIEIICsRtNQELQEINRVyKEMYKtDLEKDIIsDtsGDF |
| P07355 | Y188 | Sugiyama | ANXA2 ANX2 ANX2L4 CAL1H LPC2D | RKLMVALAKGRRAEDGsVIDyELIDQDARDLyDAGVKRKGT |
| P07355 | Y199 | Sugiyama | ANXA2 ANX2 ANX2L4 CAL1H LPC2D | RAEDGsVIDyELIDQDARDLyDAGVKRKGTDVPKWIsIMTE |
| P07355 | Y333 | Sugiyama | ANXA2 ANX2 ANX2L4 CAL1H LPC2D | KsLyyyIQQDTKGDyQKALLyLCGGDD______________ |
| P07384 | Y42 | Sugiyama | CAPN1 CANPL1 PIG30 | RARELGLGRHENAIKyLGQDyEQLRVRCLQSGTLFRDEAFP |
| P07437 | T107 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | PDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKEAESC |
| P07437 | Y106 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | RPDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKEAES |
| P07437 | Y50 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | IDPTGtyHGDsDLQLDRIsVyyNEAtGGKyVPRAILVDLEP |
| P07437 | Y51 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | DPTGtyHGDsDLQLDRIsVyyNEAtGGKyVPRAILVDLEPG |
| P07437 | Y59 | Sugiyama | TUBB TUBB5 OK/SW-cl.56 | DsDLQLDRIsVyyNEAtGGKyVPRAILVDLEPGtMDsVRsG |
| P07686 | Y526 | Sugiyama | HEXB HCC7 | ASAVGERLWSSKDVRDMDDAyDRLTRHRCRMVERGIAAQPL |
| P07686 | Y547 | Sugiyama | HEXB HCC7 | DRLTRHRCRMVERGIAAQPLyAGyCNHENM___________ |
| P07686 | Y550 | Sugiyama | HEXB HCC7 | TRHRCRMVERGIAAQPLyAGyCNHENM______________ |
| P07711 | Y112 | Sugiyama | CTSL CTSL1 | MNGFQNRKPRKGKVFQEPLFyEAPRSVDWREKGyVTPVKNQ |
| P07711 | Y311 | Sugiyama | CTSL CTSL1 | DNNKYWLVKNsWGEEWGMGGyVKMAKDRRNHCGIAsAAsyP |
| P07711 | Y330 | Sugiyama | CTSL CTSL1 | GyVKMAKDRRNHCGIAsAAsyPtV_________________ |
| P07737 | Y129 | Sugiyama | PFN1 | tLVLLMGKEGVHGGLINKKCyEMAsHLRRsQY_________ |
| P07814 | Y1504 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | KPLCELQPGAKCVCGKNPAKyytLFGRsy____________ |
| P07814 | Y1505 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | PLCELQPGAKCVCGKNPAKyytLFGRsy_____________ |
| P07814 | Y684 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | LKKGDIIQLQRRGFFICDQPyEPVsPysCKEAPCVLIyIPD |
| P07814 | Y690 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | IQLQRRGFFICDQPyEPVsPysCKEAPCVLIyIPDGHtKEM |
| P07814 | Y827 | Sugiyama | EPRS1 EPRS GLNS PARS QARS QPRS PIG32 | EIGQNIssNssAsILESKsLyDEVAAQGEVVRKLKAEKSPK |
| P07858 | Y244 | Sugiyama | CTSB CPSB | HYGYNSYSVSNSEKDIMAEIyKNGPVEGAFSVYSDFLLYKS |
| P07900 | Y197 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | GEPMGRGTKVILHLKEDQtEyLEERRIKEIVKKHSQFIGyP |
| P07900 | Y284 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | DEEEEKKDGDKKKKKKIKEKyIDQEELNKtKPIWtRNPDDI |
| P07900 | Y309 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | ELNKtKPIWtRNPDDItNEEyGEFyKsLtNDWEDHLAVKHF |
| P07900 | Y313 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | tKPIWtRNPDDItNEEyGEFyKsLtNDWEDHLAVKHFSVEG |
| P07900 | Y438 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | KKCLELFtELAEDKENyKKFyEQFSKNIKLGIHEDsQNRKK |
| P07900 | Y465 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | IKLGIHEDsQNRKKLsELLRyytsAsGDEMVsLKDYCTRMK |
| P07900 | Y466 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | KLGIHEDsQNRKKLsELLRyytsAsGDEMVsLKDYCTRMKE |
| P07900 | Y492 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | DEMVsLKDYCTRMKENQKHIyyItGETKDQVANsAFVERLR |
| P07900 | Y493 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | EMVsLKDYCTRMKENQKHIyyItGETKDQVANsAFVERLRK |
| P07900 | Y61 | Sugiyama | HSP90AA1 HSP90A HSPC1 HSPCA | KEIFLRELIsNssDALDKIRyEsLtDPsKLDsGKELHINLI |
| P07942 | Y445 | Sugiyama | LAMB1 | QCRCKLNVEGEHCDVCKEGFyDLssEDPFGCKSCACNPLGT |
| P07948 | S11 | Sugiyama | LYN JTK8 | __________MGCIKSKGKDsLsDDGVDLKTQPVRNTERTI |
| P07948 | S13 | Sugiyama | LYN JTK8 | ________MGCIKSKGKDsLsDDGVDLKTQPVRNTERTIyV |
| P07948 | S457 | Sugiyama | LYN JTK8 | VTYGKIPYPGRTNADVMTALsQGyRMPRVENCPDELyDIMK |
| P07948 | T398 | Sugiyama | LYN JTK8 | SLMCKIADFGLARVIEDNEytAREGAKFPIKWTAPEAINFG |
| P07948 | Y117 | Sugiyama | LYN JTK8 | GEWWKAKSLLTKKEGFIPSNyVAKLNTLETEEWFFKDITRK |
| P07948 | Y193 | Sugiyama | LYN JTK8 | DPVHGDVIKHYKIRsLDNGGyyISPRITFPCISDMIKHYQK |
| P07948 | Y194 | Sugiyama | LYN JTK8 | PVHGDVIKHYKIRsLDNGGyyISPRITFPCISDMIKHYQKQ |
| P07948 | Y306 | Sugiyama | LYN JTK8 | AFLEEANLMKTLQHDKLVRLyAVVTREEPIyIITEyMAKGS |
| P07948 | Y316 | Sugiyama | LYN JTK8 | TLQHDKLVRLyAVVTREEPIyIITEyMAKGSLLDFLKSDEG |
| P07948 | Y32 | Sugiyama | LYN JTK8 | LsDDGVDLKTQPVRNTERTIyVRDPTSNKQQRPVPESQLLP |
| P07948 | Y321 | Sugiyama | LYN JTK8 | KLVRLyAVVTREEPIyIITEyMAKGSLLDFLKSDEGGKVLL |
| P07948 | Y397 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP|Sugiyama | LYN JTK8 | ESLMCKIADFGLARVIEDNEytAREGAKFPIKWTAPEAINF |
| P07948 | Y460 | Sugiyama | LYN JTK8 | GKIPYPGRTNADVMTALsQGyRMPRVENCPDELyDIMKMCW |
| P07948 | Y473 | Sugiyama | LYN JTK8 | MTALsQGyRMPRVENCPDELyDIMKMCWKEKAEERPTFDYL |
| P07948 | Y508 | GPS6|EPSD|PSP | LYN JTK8 | PTFDYLQsVLDDFytAtEGQyQQQP________________ |
| P07951 | Y261 | Sugiyama | TPM2 TMSB | FAERsVAKLEKtIDDLEDEVyAQKMKYKAIsEELDNALNDI |
| P07954 | Y110 | Sugiyama | FH | tPVIKAFGILKRAAAEVNQDyGLDPKIANAIMKAADEVAEG |
| P07954 | Y54 | Sugiyama | FH | PSFWPPNAARMAsQNSFRIEyDtFGELKVPNDKYYGAQTVR |
| P08238 | S462 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | HEDstNRRRLsELLRyHtsQsGDEMtsLsEyVsRMKEtQKs |
| P08238 | Y192 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | GEPIGRGTKVILHLKEDQtEyLEERRVKEVVKKHsQFIGyP |
| P08238 | Y276 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | DEEDDsGKDKKKKTKKIKEKyIDQEELNKtKPIWtRNPDDI |
| P08238 | Y301 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | ELNKtKPIWtRNPDDItQEEyGEFyKsLtNDWEDHLAVKHF |
| P08238 | Y305 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | tKPIWtRNPDDItQEEyGEFyKsLtNDWEDHLAVKHFSVEG |
| P08238 | Y430 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | KKCLELFsELAEDKENyKKFyEAFSKNLKLGIHEDstNRRR |
| P08238 | Y472 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | sELLRyHtsQsGDEMtsLsEyVsRMKEtQKsIyyItGEsKE |
| P08238 | Y484 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | DEMtsLsEyVsRMKEtQKsIyyItGEsKEQVANsAFVERVR |
| P08238 | Y485 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | EMtsLsEyVsRMKEtQKsIyyItGEsKEQVANsAFVERVRK |
| P08238 | Y512 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | EQVANsAFVERVRKRGFEVVyMtEPIDEyCVQQLKEFDGKs |
| P08238 | Y520 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | VERVRKRGFEVVyMtEPIDEyCVQQLKEFDGKsLVsVtKEG |
| P08238 | Y56 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | KEIFLRELIsNAsDALDKIRyEsLtDPsKLDsGKELKIDII |
| P08238 | Y619 | Sugiyama | HSP90AB1 HSP90B HSPC2 HSPC3 HSPCB | TANMERIMKAQALRDNstMGyMMAKKHLEINPDHPIVEtLR |
| P08621 | Y126 | Sugiyama | SNRNP70 RNPU1Z RPU1 SNRP70 U1AP1 | FVARVNYDTTEsKLRREFEVyGPIKRIHMVYSKRsGKPRGy |
| P08631 | T412 | Sugiyama | HCK | SLVCKIADFGLARVIEDNEytAREGAKFPIKWTAPEAINFG |
| P08631 | Y411 | Sugiyama | HCK | ASLVCKIADFGLARVIEDNEytAREGAKFPIKWTAPEAINF |
| P08670 | Y291 | Sugiyama | VIM | DVRQQyEsVAAKNLQEAEEWyKSKFADLsEAANRNNDALRQ |
| P08670 | Y53 | Sugiyama | VIM | tsTRtYsLGsALRPstsRsLyAssPGGVyAtRssAVRLRss |
| P08670 | Y61 | Sugiyama | VIM | GsALRPstsRsLyAssPGGVyAtRssAVRLRssVPGVRLLQ |
| P08708 | Y84 | Sugiyama | RPS17 RPS17L | GPVRGISIKLQEEERERRDNyVPEVsALDQEIIEVDPDtKE |
| P08758 | S135 | Sugiyama | ANXA5 ANX5 ENX2 PP4 | AsRtPEELRAIKQVyEEEyGssLEDDVVGDTSGYYQRMLVV |
| P08758 | Y129 | Sugiyama | ANXA5 ANX5 ENX2 PP4 | VLtEIIAsRtPEELRAIKQVyEEEyGssLEDDVVGDTSGYY |
| P08758 | Y133 | Sugiyama | ANXA5 ANX5 ENX2 PP4 | IIAsRtPEELRAIKQVyEEEyGssLEDDVVGDTSGYYQRML |
| P08758 | Y91 | Sugiyama | ANXA5 ANX5 ENX2 PP4 | SELTGKFEKLIVALMKPSRLyDAyELKHALKGAGTNEKVLt |
| P08758 | Y94 | Sugiyama | ANXA5 ANX5 ENX2 PP4 | TGKFEKLIVALMKPSRLyDAyELKHALKGAGTNEKVLtEII |
| P09104 | T41 | Sugiyama | ENO2 | EVDLyTAKGLFRAAVPsGAstGIyEALELRDGDKQRYLGKG |
| P09104 | Y44 | Sugiyama | ENO2 | LyTAKGLFRAAVPsGAstGIyEALELRDGDKQRYLGKGVLK |
| P09211 | Y50 | Sugiyama | GSTP1 FAEES3 GST3 | KEEVVTVETWQEGsLKASCLyGQLPKFQDGDLtLyQsNtIL |
| P09234 | Y12 | Sugiyama | SNRPC | _________MPKFyCDyCDtyLtHDsPsVRKTHCSGRKHKE |
| P09496 | Y147 | Sugiyama | CLTA | NSRKQEAEWKEKAIKELEEWyARQDEQLQKTKANNRVADEA |
| P09651 | S338 | Sugiyama | HNRNPA1 HNRPA1 | YNNQSSNFGPMKGGNFGGRssGPyGGGGQyFAKPRNQGGyG |
| P09651 | Y341 | Sugiyama | HNRNPA1 HNRPA1 | QSSNFGPMKGGNFGGRssGPyGGGGQyFAKPRNQGGyGGss |
| P09651 | Y347 | Sugiyama | HNRNPA1 HNRPA1 | PMKGGNFGGRssGPyGGGGQyFAKPRNQGGyGGssssssyG |
| P09923 | Y179 | Sugiyama | ALPI | GKSVGVVTTTRVQHAsPAGtyAHtVNRNWysDADMPASARQ |
| P09960 | Y233 | Sugiyama | LTA4H LTA4 | RQIGPRTLVWSEKEQVEKSAyEFsETEsMLKIAEDLGGPYV |
| P09972 | Y358 | Sugiyama | ALDOC ALDC | AAQGKYEGSGEDGGAAAQsLyIANHAY______________ |
| P0CG38 | Y1062 | Sugiyama | POTEI | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P0CG38 | Y791 | Sugiyama | POTEI | MEHGIITNWDDMEKIWHHtFyNELRVAPEEHPILLTEAPLN |
| P0CG39 | Y1025 | Sugiyama | POTEJ | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P0CG39 | Y754 | Sugiyama | POTEJ | MEHGIITNWDDMEKIWHHtFyNELRVAPEEHPILLTEAPLN |
| P0CL80 | Y10 | Sugiyama | GAGE12F | ___________MSWRGRsTyyWPRPRRYVQPPEMIGPMRPE |
| P0CL80 | Y9 | Sugiyama | GAGE12F | ____________MSWRGRsTyyWPRPRRYVQPPEMIGPMRP |
| P0DPH7 | T225 | Sugiyama | TUBA3C TUBA2 | DNEAIYDICRRNLDIERPtytNLNRLIGQIVSSITASLRFD |
| P0DPH7 | Y103 | Sugiyama | TUBA3C TUBA2 | yRQLFHPEQLItGKEDAANNyARGHYTIGKEIVDLVLDRIR |
| P0DSO3 | Y10 | Sugiyama | GAGE4 | ___________MSWRGRsTyyWPRPRRYVQPPEMIGPMRPE |
| P0DSO3 | Y9 | Sugiyama | GAGE4 | ____________MSWRGRsTyyWPRPRRYVQPPEMIGPMRP |
| P10809 | Y223 | Sugiyama | HSPD1 HSP60 | DGKtLNDELEIIEGMKFDRGyIsPyFINtsKGQKCEFQDAy |
| P10809 | Y227 | Sugiyama | HSPD1 HSP60 | LNDELEIIEGMKFDRGyIsPyFINtsKGQKCEFQDAyVLLs |
| P10809 | Y243 | Sugiyama | HSPD1 HSP60 | yIsPyFINtsKGQKCEFQDAyVLLsEKKIssIQsIVPALEI |
| P11047 | Y352 | Sugiyama | LAMC1 LAMB2 | tAEsASECLPCDCNGRsQECyFDPELyRSTGHGGHCTNCQD |
| P11137 | Y67 | GPS6|ELM|iPTMNet|EPSD | MAP2 | GFPyREDEEGAFGEHGSQGTySNTKENGINGELTSADRETA |
| P11142 | T427 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | GGVMTVLIKRNtTIPTKQtQtFttysDNQPGVLIQVyEGER |
| P11142 | T45 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | KVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVAMNPtN |
| P11142 | Y134 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | FYPEEVSSMVLTKMKEIAEAyLGKtVTNAVVtVPAyFNDsQ |
| P11142 | Y149 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | EIAEAyLGKtVTNAVVtVPAyFNDsQRQAtKDAGtIAGLNV |
| P11142 | Y41 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | FQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVAM |
| P11142 | Y443 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | KQtQtFttysDNQPGVLIQVyEGERAMTKDNNLLGKFELTG |
| P11142 | Y545 | Sugiyama | HSPA8 HSC70 HSP73 HSPA10 | YKAEDEKQRDKVssKNsLEsyAFNMKATVEDEKLQGKINDE |
| P11274 | Y177 | EPSD|PSP | BCR BCR1 D22S11 | NFERIRKGHGQPGADAEKPFyVNVEFHHERGLVKVNDKEVS |
| P11310 | Y67 | Sugiyama | ACADM | EFQATARKFAREEIIPVAAEyDKTGEyPVPLIRRAWELGLM |
| P11498 | Y118 | Sugiyama | PC | HIPDIIKVAKENNVDAVHPGyGFLsERADFAQACQDAGVRF |
| P11498 | Y84 | Sugiyama | PC | VAIYSEQDTGQMHRQKADEAyLIGRGLAPVQAYLHIPDIIK |
| P11802 | Y17 | EPSD|PSP | CDK4 | ____MATSRYEPVAEIGVGAyGTVYKARDPHsGHFVALKSV |
| P11912 | Y188 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | CD79A IGA MB1 | RWQNEKLGLDAGDEyEDENLyEGLNLDDCSMyEDISRGLQG |
| P11940 | Y194 | Sugiyama | PABPC1 PAB1 PABP PABP1 PABPC2 | KSRKEREAELGARAKEFtNVyIKNFGEDMDDERLKDLFGKF |
| P11940 | Y297 | Sugiyama | PABPC1 PAB1 PABP PABP1 PABPC2 | KRKFEQMKQDRITRyQGVNLyVKNLDDGIDDERLRKEFsPF |
| P12277 | Y125 | Sugiyama | CKB CKBB | EHKTDLNPDNLQGGDDLDPNyVLssRVRTGRSIRGFCLPPH |
| P12277 | Y39 | Sugiyama | CKB CKBB | EFPDLSAHNNHMAKVLtPELyAELRAKSTPSGFTLDDVIQT |
| P12318 | Y281 | GPS6|ELM|iPTMNet|EPSD | FCGR2A CD32 FCG2 FCGR2A1 IGFR2 | PPGRQMIAIRKRQLEETNNDyEtADGGyMtLNPRAPTDDDK |
| P12318 | Y288 | GPS6|ELM|iPTMNet|EPSD | FCGR2A CD32 FCG2 FCGR2A1 IGFR2 | AIRKRQLEETNNDyEtADGGyMtLNPRAPTDDDKNIyLTLP |
| P12318 | Y304 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | FCGR2A CD32 FCG2 FCGR2A1 IGFR2 | ADGGyMtLNPRAPTDDDKNIyLTLPPNDHVNSNN_______ |
| P12814 | Y215 | Sugiyama | ACTN1 | KLRKDDPLTNLNTAFDVAEKyLDIPKMLDAEDIVGtARPDE |
| P12814 | Y378 | Sugiyama | ACTN1 | GRMVSDINNAWGCLEQVEKGyEEWLLNEIRRLERLDHLAEK |
| P12814 | Y859 | Sugiyama | ACTN1 | DKNyITMDELRRELPPDQAEyCIARMAPYTGPDSVPGALDY |
| P12956 | Y530 | Sugiyama | XRCC6 G22P1 | KVEAMNKRLGsLVDEFKELVyPPDyNPEGKVtKRKHDNEGS |
| P12956 | Y534 | Sugiyama | XRCC6 G22P1 | MNKRLGsLVDEFKELVyPPDyNPEGKVtKRKHDNEGSGSKR |
| P13073 | Y38 | Sugiyama | COX4I1 COX4 | SVCVRAHESVVKsEDFsLPAyMDRRDHPLPEVAHVKHLSAS |
| P13639 | S732 | Sugiyama | EEF2 EF2 | DAIHRGGGQIIPtARRCLyAsVLtAQPRLMEPIyLVEIQCP |
| P13639 | Y367 | Sugiyama | EEF2 EF2 | GDALLQMITIHLPSPVTAQKyRCELLyEGPPDDEAAMGIKs |
| P13639 | Y373 | Sugiyama | EEF2 EF2 | MITIHLPSPVTAQKyRCELLyEGPPDDEAAMGIKsCDPKGP |
| P13639 | Y443 | Sugiyama | EEF2 EF2 | TGLKVRIMGPNytPGKKEDLyLKPIQRTILMMGRYVEPIED |
| P13639 | Y634 | Sugiyama | EEF2 EF2 | AEDIDKGEVsARQELKQRARyLAEKyEWDVAEARKIWCFGP |
| P13639 | Y639 | Sugiyama | EEF2 EF2 | KGEVsARQELKQRARyLAEKyEWDVAEARKIWCFGPDGTGP |
| P13639 | Y671 | Sugiyama | EEF2 EF2 | CFGPDGTGPNILTDITKGVQyLNEIKDSVVAGFQWATKEGA |
| P13639 | Y730 | Sugiyama | EEF2 EF2 | HADAIHRGGGQIIPtARRCLyAsVLtAQPRLMEPIyLVEIQ |
| P13667 | T449 | Sugiyama | PDIA4 ERP70 ERP72 | AATQFWRSKVLEVAKDFPEytFAIADEEDyAGEVKDLGLsE |
| P13667 | Y137 | Sugiyama | PDIA4 ERP70 ERP72 | VAKIDAtsAsVLAsRFDVsGyPtIKILKKGQAVDyEGsRtQ |
| P13667 | Y273 | Sugiyama | PDIA4 ERP70 ERP72 | PTLKIFRKGRPYDYNGPREKyGIVDyMIEQSGPPSKEILTL |
| P13667 | Y278 | Sugiyama | PDIA4 ERP70 ERP72 | FRKGRPYDYNGPREKyGIVDyMIEQSGPPSKEILTLKQVQE |
| P13667 | Y392 | Sugiyama | PDIA4 ERP70 ERP72 | HMMDVQGstQDsAIKDFVLKyALPLVGHRKVSNDAKRYTRR |
| P13667 | Y448 | Sugiyama | PDIA4 ERP70 ERP72 | RAATQFWRSKVLEVAKDFPEytFAIADEEDyAGEVKDLGLs |
| P13667 | Y458 | Sugiyama | PDIA4 ERP70 ERP72 | VLEVAKDFPEytFAIADEEDyAGEVKDLGLsEsGEDVNAAI |
| P13667 | Y565 | Sugiyama | PDIA4 ERP70 ERP72 | DVLIEFYAPWCGHCKQLEPVyNsLAKKYKGQKGLVIAKMDA |
| P13674 | Y141 | Sugiyama | P4HA1 P4HA | FPNDEDQVGAAKALLRLQDtyNLDTDtIsKGNLPGVKHKSF |
| P13674 | Y247 | Sugiyama | P4HA1 P4HA | LTKKLLELDPEHQRANGNLKyFEyIMAKEKDVNKSASDDQS |
| P13674 | Y250 | Sugiyama | P4HA1 P4HA | KLLELDPEHQRANGNLKyFEyIMAKEKDVNKSASDDQSDQK |
| P13674 | Y282 | Sugiyama | P4HA1 P4HA | ASDDQSDQKTTPKKKGVAVDyLPERQKyEMLCRGEGIKMTP |
| P13693 | Y18 | Sugiyama | TPT1 | ___MIIYRDLIsHDEMFsDIyKIREIADGLCLEVEGKMVSR |
| P13798 | S187 | Sugiyama | APEH D3F15S2 D3S48E DNF15S2 | EKKRPKAEsFFQTKALDVsAsDDEIARLKKPDQAIKGDQFV |
| P13798 | Y17 | Sugiyama | APEH D3F15S2 D3S48E DNF15S2 | ____MERQVLLsEPEEAAALyRGLSRQPALsAACLGPEVtT |
| P13929 | T41 | Sugiyama | ENO3 | EVDLHtAKGRFRAAVPsGAstGIyEALELRDGDKGRYLGKG |
| P13929 | Y44 | Sugiyama | ENO3 | LHtAKGRFRAAVPsGAstGIyEALELRDGDKGRYLGKGVLK |
| P13987 | Y86 | Sugiyama | CD59 MIC11 MIN1 MIN2 MIN3 MSK21 | KFEHCNFNDVtTRLRENELtyyCCKKDLCNFNEQLENGGTS |
| P13987 | Y87 | Sugiyama | CD59 MIC11 MIN1 MIN2 MIN3 MSK21 | FEHCNFNDVtTRLRENELtyyCCKKDLCNFNEQLENGGTSL |
| P14314 | T469 | Sugiyama | PRKCSH G19P1 | WGsWIGPDHDKFSAMKyEQGtGCWQGPNRstTVRLLCGKEt |
| P14314 | Y106 | Sugiyama | PRKCSH G19P1 | yIPSNRVNDGVCDCCDGtDEyNsGVICENtCKEKGRKEREs |
| P14314 | Y465 | Sugiyama | PRKCSH G19P1 | sLGtWGsWIGPDHDKFSAMKyEQGtGCWQGPNRstTVRLLC |
| P14317 | Y222 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | HCLS1 HS1 | KDRVDKSAVGFNEMEAPTTAyKKTTPIEAASSGTRGLKAKF |
| P14317 | Y378 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | HCLS1 HS1 | PVYEAEPEPEPEPEPEPENDyEDVEEMDRHEQEDEPEGDyE |
| P14317 | Y397 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | HCLS1 HS1 | DyEDVEEMDRHEQEDEPEGDyEEVLEPEDSSFSSALAGSSG |
| P14618 | Y148 | Sugiyama | PKM OIP3 PK2 PK3 PKM2 | GtAEVELKKGATLKITLDNAyMEKCDENILWLDYKNICKVV |
| P14625 | Y258 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | GNTLGRGTTITLVLKEEAsDyLELDTIKNLVKKYSQFINFP |
| P14625 | Y401 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | VTFKSILFVPTSAPRGLFDEyGsKKSDYIKLYVRRVFITDD |
| P14625 | Y429 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | IKLYVRRVFITDDFHDMMPKyLNFVKGVVDsDDLPLNVsRE |
| P14625 | Y527 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | AKLLRFQssHHPtDItsLDQyVERMKEKQDKIyFMAGsSRK |
| P14625 | Y539 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | tDItsLDQyVERMKEKQDKIyFMAGsSRKEAEssPFVERLL |
| P14625 | Y678 | Sugiyama | HSP90B1 GRP94 HSPC4 TRA1 | MERIMKAQAYQtGKDIstNyyAsQKKTFEINPRHPLIRDML |
| P14635 | Y175 | Sugiyama | CCNB1 CCNB | DVDAEDGADPNLCSEYVKDIyAYLRQLEEEQAVRPKYLLGR |
| P14649 | S87 | Sugiyama | MYL6B MLC1SA | EEFKEAFELFDRVGDGKILysQCGDVMRALGQNPtNAEVLK |
| P14649 | Y86 | Sugiyama | MYL6B MLC1SA | LEEFKEAFELFDRVGDGKILysQCGDVMRALGQNPtNAEVL |
| P14854 | Y34 | Sugiyama | COX6B1 COX6B | TAPFDSRFPNQNQTRNCWQNyLDFHRCQKAMTAKGGDIsVC |
| P14854 | Y57 | Sugiyama | COX6B1 COX6B | FHRCQKAMTAKGGDIsVCEWyQRVYQsLCPtsWVTDWDEQR |
| P14927 | Y56 | Sugiyama | UQCRB UQBP | DTIYEDEDVKEAIRRLPENLyNDRMFRIKRALDLNLKHQIL |
| P15259 | Y92 | Sugiyama | PGAM2 PGAMM | DGTDQMWLPVVRTWRLNERHyGGLtGLNKAETAAKHGEEQV |
| P15311 | Y424 | Sugiyama | EZR VIL2 | ERQAVDQIKsQEQLAAELAEytAKIALLEEARRRKEDEVEE |
| P15328 | Y80 | Sugiyama | FOLR1 FOLR | WRKNACCSTNTSQEAHKDVsyLyRFNWNHCGEMAPACKRHF |
| P15374 | Y141 | Sugiyama | UCHL3 | KFLEEsVsMsPEERARyLENyDAIRVtHEtsAHEGQTEAPs |
| P15391 | Y409 | iPTMNet|EPSD | CD19 | GALGSRSPPGVGPEEEEGEGyEEPDSEEDSEFYENDSNLGQ |
| P15391 | Y500 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | CD19 | SPHGSAWDPSREATSLGSQsyEDMRGILyAAPQLRSIRGQP |
| P15391 | Y531 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | CD19 | PQLRSIRGQPGPNHEEDADSyENMDNPDGPDPAWGGGGRMG |
| P15880 | Y248 | Sugiyama | RPS2 RPS4 | GCtAtLGNFAKATFDAISKTysyLtPDLWKEtVFtKsPyQE |
| P15880 | Y250 | Sugiyama | RPS2 RPS4 | tAtLGNFAKATFDAISKTysyLtPDLWKEtVFtKsPyQEFt |
| P16885 | Y743 | GPS6|ELM|iPTMNet|EPSD | PLCG2 | HSLYRKMRLRYPVTPELLERyNMERDINSLyDVSRMyVDPS |
| P16885 | Y753 | SIGNOR|iPTMNet|EPSD | PLCG2 | YPVTPELLERyNMERDINSLyDVSRMyVDPSEINPSMPQRT |
| P16885 | Y759 | SIGNOR|iPTMNet|EPSD | PLCG2 | LLERyNMERDINSLyDVSRMyVDPSEINPSMPQRTVKALYD |
| P17066 | T47 | Sugiyama | HSPA6 HSP70B' | RVEILANDQGNRTtPsyVAFtDtERLVGDAAKsQAALNPHN |
| P17066 | Y43 | Sugiyama | HSPA6 HSP70B' | FQQGRVEILANDQGNRTtPsyVAFtDtERLVGDAAKsQAAL |
| P17676 | Y137 | Sugiyama | CEBPB TCF5 PP9092 | FLSDLFSDDYGGKNCKKPAEyGyVsLGRLGAAKGALHPGCF |
| P17676 | Y139 | Sugiyama | CEBPB TCF5 PP9092 | SDLFSDDYGGKNCKKPAEyGyVsLGRLGAAKGALHPGCFAP |
| P17812 | Y468 | Sugiyama | CTPS1 CTPS | MRLGKRRtLFQTKNsVMRKLyGDADyLEERHRHRFEVNPVW |
| P17812 | Y473 | Sugiyama | CTPS1 CTPS | RRtLFQTKNsVMRKLyGDADyLEERHRHRFEVNPVWKKCLE |
| P17980 | Y381 | Sugiyama | PSMC3 TBP1 | ARARIMQIHSRKMNVsPDVNyEELARCTDDFNGAQCKAVCV |
| P17987 | Y545 | Sugiyama | TCP1 CCT1 CCTA | LRIDDLIKLHPESKDDKHGsyEDAVHsGALND_________ |
| P18077 | Y106 | Sugiyama | RPL35A GIG33 | AKFRsNLPAKAIGHRIRVMLyPSRI________________ |
| P18124 | Y155 | Sugiyama | RPL7 | IVEPYIAWGYPNLKsVNELIyKRGYGKINKKRIALtDNALI |
| P18206 | Y822 | Sugiyama | VCL | KAVAGNIsDPGLQKsFLDsGyRILGAVAKVREAFQPQEPDF |
| P18615 | Y133 | Sugiyama | NELFE RD RDBP | sIsADDDLQEsSRRPQRKsLyEsFVsssDRLRELGPDGEEA |
| P18615 | Y170 | Sugiyama | NELFE RD RDBP | GEEAEGPGAGDGPPRsFDWGyEERSGAHSsAsPPRsRSRDR |
| P18621 | S5 | Sugiyama | RPL17 | ________________MVRysLDPENPtKsCKSRGSNLRVH |
| P18621 | Y4 | Sugiyama | RPL17 | _________________MVRysLDPENPtKsCKSRGSNLRV |
| P18669 | S134 | Sugiyama | PGAM1 PGAMA CDABP0006 | IWRRsyDVPPPPMEPDHPFysNIsKDRRyADLtEDQLPsCE |
| P18669 | S137 | Sugiyama | PGAM1 PGAMA CDABP0006 | RsyDVPPPPMEPDHPFysNIsKDRRyADLtEDQLPsCEsLK |
| P18669 | Y119 | Sugiyama | PGAM1 PGAMA CDABP0006 | NKAETAAKHGEAQVKIWRRsyDVPPPPMEPDHPFysNIsKD |
| P18669 | Y142 | Sugiyama | PGAM1 PGAMA CDABP0006 | PPPPMEPDHPFysNIsKDRRyADLtEDQLPsCEsLKDtIAR |
| P18669 | Y26 | Sugiyama | PGAM1 PGAMA CDABP0006 | LVLIRHGEsAWNLENRFsGWyDADLsPAGHEEAKRGGQALR |
| P18669 | Y92 | Sugiyama | PGAM1 PGAMA CDABP0006 | DAIDQMWLPVVRTWRLNERHyGGLtGLNKAETAAKHGEAQV |
| P18754 | Y89 | Sugiyama | RCC1 CHC1 | VVQAEAGGMHTVCLSKsGQVysFGCNDEGALGRDtsVEGSE |
| P19105 | Y142 | Sugiyama | MYL12A MLCB MRLC3 RLC | LRELLttMGDRFtDEEVDELyREAPIDKKGNFNyIEFtRIL |
| P19105 | Y155 | Sugiyama | MYL12A MLCB MRLC3 RLC | DEEVDELyREAPIDKKGNFNyIEFtRILKHGAKDKDD____ |
| P19174 | Y771 | SIGNOR|iPTMNet|EPSD | PLCG1 PLC1 | KLRYPINEEALEKIGTAEPDyGALyEGRNPGFyVEANPMPT |
| P19174 | Y783 | SIGNOR|iPTMNet|EPSD | PLCG1 PLC1 | KIGTAEPDyGALyEGRNPGFyVEANPMPTFKCAVKALFDYK |
| P19235 | Y368 | GPS6|ELM|iPTMNet|EPSD | EPOR | GTDDEGPLLEPVGSEHAQDTyLVLDKWLLPRNPPSEDLPGP |
| P19338 | Y462 | Sugiyama | NCL | AEKTFEEKQGtEIDGRsIsLyytGEKGQNQDYRGGKNSTWs |
| P20042 | Y174 | Sugiyama | EIF2S2 EIF2B | DDGIsFsNQtGPAWAGSERDytyEELLNRVFNIMREKNPDM |
| P20042 | Y176 | Sugiyama | EIF2S2 EIF2B | GIsFsNQtGPAWAGSERDytyEELLNRVFNIMREKNPDMVA |
| P20618 | S151 | Sugiyama | PSMB1 PSC5 | PYYVYNIIGGLDEEGKGAVysFDPVGsyQRDsFKAGGSASA |
| P20618 | Y150 | Sugiyama | PSMB1 PSC5 | FPYYVYNIIGGLDEEGKGAVysFDPVGsyQRDsFKAGGSAS |
| P20618 | Y158 | Sugiyama | PSMB1 PSC5 | IGGLDEEGKGAVysFDPVGsyQRDsFKAGGSASAMLQPLLD |
| P21127 | Y449 | Sugiyama | CDK11B CDC2L1 CDK11 PITSLREA PK58 | LQGCRsVEEFQCLNRIEEGtyGVVYRAKDKKTDEIVALKRL |
| P21333 | Y1519 | Sugiyama | FLNA FLN FLN1 | VVDNADGTQTVNyVPSREGPysIsVLyGDEEVPRsPFKVKV |
| P21333 | Y1525 | Sugiyama | FLNA FLN FLN1 | GTQTVNyVPSREGPysIsVLyGDEEVPRsPFKVKVLPTHDA |
| P21333 | Y1632 | Sugiyama | FLNA FLN FLN1 | VTGRYTILIKYGGDEIPFsPyRVRAVPTGDASKCTVTVSIG |
| P21333 | Y373 | Sugiyama | FLNA FLN FLN1 | THKVTVLFAGQHIAKsPFEVyVDKsQGDASKVTAQGPGLEP |
| P21333 | Y731 | Sugiyama | FLNA FLN FLN1 | VQDNEGCPVEALVKDNGNGtysCSyVPRKPVKHTAMVSWGG |
| P21980 | Y369 | Sugiyama | TGM2 | PGYEGWQALDPTPQEKsEGtyCCGPVPVRAIKEGDLstKyD |
| P22059 | Y767 | Sugiyama | OSBP OSBP1 | RKKREAEAMKATEDGtPYDPyKALWFERKKDPVTKELTHIy |
| P22234 | Y22 | Sugiyama | PAICS ADE2 AIRC PAIS | AtAEVLNIGKKLYEGKtKEVyELLDsPGKVLLQsKDQItAG |
| P22314 | Y55 | Sugiyama | UBA1 A1S9T UBE1 | SVPTNGMAKNGsEADIDEGLysRQLyVLGHEAMKRLQTSSV |
| P22392 | Y151 | Sugiyama | NME2 NM23B | SLWFKPEELVDyKSCAHDWVyE___________________ |
| P22626 | Y331 | Sugiyama | HNRNPA2B1 HNRPA2B1 | SNYGPMKsGNFGGsRNMGGPyGGGNyGPGGsGGsGGyGGRs |
| P22681 | Y371 | EPSD|PSP | CBL CBL2 RNF55 | GLCEPTPQDHIKVTQEQyELyCEMGSTFQLCKICAENDKDV |
| P23246 | Y488 | Sugiyama | SFPQ PSF | PMYQKEREtPPRFAQHGtFEyEysQRWKsLDEMEKQQREQV |
| P23246 | Y490 | Sugiyama | SFPQ PSF | YQKEREtPPRFAQHGtFEyEysQRWKsLDEMEKQQREQVEK |
| P23284 | Y119 | Sugiyama | PPIB CYPB | DFMIQGGDFtRGDGtGGKsIyGERFPDENFKLKHyGPGWVs |
| P23434 | Y139 | Sugiyama | GCSH | EVTEINEALAENPGLVNKSCyEDGWLIKMtLsNPsELDELM |
| P23434 | Y164 | Sugiyama | GCSH | LIKMtLsNPsELDELMsEEAyEKYIKSIEE___________ |
| P23526 | Y165 | Sugiyama | AHCY SAHH | QLLPGIRGIsEEtTTGVHNLyKMMANGILKVPAINVNDsVt |
| P23526 | Y193 | Sugiyama | AHCY SAHH | LKVPAINVNDsVtKsKFDNLyGCRESLIDGIKRATDVMIAG |
| P23527 | Y41 | Sugiyama | H2BC17 H2BFH H2BFN HIST1H2BO | KAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P23527 | Y43 | Sugiyama | H2BC17 H2BFH H2BFN HIST1H2BO | QKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGISSKAMGIM |
| P23528 | Y140 | Sugiyama | CFL1 CFL | SKDAIKKKLtGIKHELQANCyEEVKDRCTLAEKLGGsAVIs |
| P23528 | Y68 | Sugiyama | CFL1 CFL | ILEEGKEILVGDVGQtVDDPyAtFVKMLPDKDCRyALyDAt |
| P23528 | Y82 | Sugiyama | CFL1 CFL | QtVDDPyAtFVKMLPDKDCRyALyDAtyEtKESKKEDLVFI |
| P23528 | Y85 | Sugiyama | CFL1 CFL | DDPyAtFVKMLPDKDCRyALyDAtyEtKESKKEDLVFIFWA |
| P23528 | Y89 | Sugiyama | CFL1 CFL | AtFVKMLPDKDCRyALyDAtyEtKESKKEDLVFIFWAPESA |
| P23588 | Y211 | Sugiyama | EIF4B | DsDKtDTDWRARPAtDsFDDyPPRRGDDsFGDKYRDRYDsD |
| P23588 | Y593 | Sugiyama | EIF4B | APEPKKPEENPASKFssASKyAALsVDGEDENEGEDyAE__ |
| P23921 | Y553 | Sugiyama | RRM1 RR1 | EtIyyGALEASCDLAKEQGPyEtyEGsPVsKGILQYDMWNV |
| P23921 | Y556 | Sugiyama | RRM1 RR1 | yyGALEASCDLAKEQGPyEtyEGsPVsKGILQYDMWNVTPT |
| P24534 | Y18 | Sugiyama | EEF1B2 EEF1B EF1B | ___MGFGDLKsPAGLQVLNDyLADKSYIEGYVPsQADVAVF |
| P24752 | Y188 | Sugiyama | ACAT1 ACAT MAT | TPYGGVKLEDLIVKDGLtDVyNKIHMGsCAENTAKKLNIAR |
| P24752 | Y214 | Sugiyama | ACAT1 ACAT MAT | GsCAENTAKKLNIARNEQDAyAINsytRSKAAWEAGKFGNE |
| P24752 | Y256 | Sugiyama | ACAT1 ACAT MAT | IPVtVtVKGQPDVVVKEDEEyKRVDFSKVPKLKTVFQKENG |
| P24844 | Y156 | Sugiyama | MYL9 MLC2 MRLC1 MYRL2 | DEEVDEMyREAPIDKKGNFNyVEFTRILKHGAKDKDD____ |
| P24941 | Y15 | Sugiyama | CDK2 CDKN2 | ______MENFQKVEKIGEGtyGVVyKARNKLTGEVVALKKI |
| P24941 | Y19 | Sugiyama | CDK2 CDKN2 | __MENFQKVEKIGEGtyGVVyKARNKLTGEVVALKKIRLDt |
| P25205 | Y32 | Sugiyama | MCM3 | LREAQRDyLDFLDDEEDQGIyQsKVRELIsDNQyRLIVNVN |
| P25205 | Y708 | Sugiyama | MCM3 | KRKRRKTRQPDAKDGDsyDPyDFsDtEEEMPQVHtPKTADs |
| P25208 | Y58 | Sugiyama | NFYB HAP3 | SMNDHEDTNGSKESFREQDIyLPIANVARIMKNAIPQTGKI |
| P25398 | Y127 | Sugiyama | RPS12 | sCVVVKDYGKESQAKDVIEEyFKCKK_______________ |
| P25490 | Y254 | SIGNOR|EPSD|PSP | YY1 INO80S | HETVVEEQIIGENsPPDysEyMtGKKLPPGGIPGIDLSDPK |
| P25490 | Y383 | SIGNOR|EPSD|PSP | YY1 INO80S | RFsLDFNLRTHVRIHtGDRPyVCPFDGCNKKFAQSTNLKSH |
| P25490 | Y8 | SIGNOR|EPSD|PSP | YY1 INO80S | _____________MASGDTLyIATDGSEMPAEIVELHEIEV |
| P25685 | Y176 | Sugiyama | DNAJB1 DNAJ1 HDJ1 HSPF1 | ARKKQDPPVTHDLRVsLEEIysGCtKKMKISHKRLNPDGKS |
| P25685 | Y52 | Sugiyama | DNAJB1 DNAJ1 HDJ1 HSPF1 | HPDKNKEPGAEEKFKEIAEAyDVLSDPRKREIFDRYGEEGL |
| P25685 | Y6 | Sugiyama | DNAJB1 DNAJ1 HDJ1 HSPF1 | _______________MGKDyyQTLGLARGAsDEEIKRAYRR |
| P25786 | Y6 | Sugiyama | PSMA1 HC2 NU PROS30 PSC2 | _______________MFRNQyDNDVtVWsPQGRIHQIEYAM |
| P25787 | Y57 | Sugiyama | PSMA2 HC3 PSC3 | GIKAANGVVLATEKKQKSILyDERSVHKVEPITKHIGLVys |
| P25788 | Y105 | Sugiyama | PSMA3 HC8 PSC8 | ARSLADIAREEAsNFRSNFGyNIPLKHLADRVAMYVHAYTL |
| P26196 | Y469 | Sugiyama | DDX6 HLR2 RCK | IEEQLGTEIKPIPsNIDKSLyVAEyHsEPVEDEKP______ |
| P26196 | Y473 | Sugiyama | DDX6 HLR2 RCK | LGTEIKPIPsNIDKSLyVAEyHsEPVEDEKP__________ |
| P26599 | Y127 | Sugiyama | PTBP1 PTB | ANTMVNYYTSVTPVLRGQPIyIQFsNHKELKtDSSPNQARA |
| P26639 | T574 | Sugiyama | TARS1 TARS | RYHQCATIQLDFQLPIRFNLtyVsHDGDDKKRPVIVHRAIL |
| P26639 | T629 | Sugiyama | TARS1 TARS | GGKWPFWLSPRQVMVVPVGPtCDEyAQKVRQQFHDAKFMAD |
| P26639 | Y633 | Sugiyama | TARS1 TARS | PFWLSPRQVMVVPVGPtCDEyAQKVRQQFHDAKFMADIDLD |
| P26640 | Y601 | Sugiyama | VARS1 G7A VARS VARS2 | VDMDFGTGAVKITPAHDQNDyEVGQRHGLEAIsIMDsRGAL |
| P26885 | Y112 | Sugiyama | FKBP2 FKBP13 | GLLGMCEGEKRKLVIPsELGyGERGAPPKIPGGATLVFEVE |
| P27348 | Y149 | Sugiyama | YWHAQ | LAEVACGDDRKQtIDNsQGAyQEAFDIsKKEMQPTHPIRLG |
| P27348 | Y48 | Sugiyama | YWHAQ | AVtEQGAELsNEERNLLsVAyKNVVGGRRSAWRVIsSIEQK |
| P27540 | Y561 | Sugiyama | ARNT BHLHE2 | PLEKSDGLFAQDRDPRFsEIyHNINADQSKGISSSTVPATQ |
| P27695 | Y45 | Sugiyama | APEX1 APE APE1 APEX APX HAP1 REF1 | KSKTAAKKNDKEAAGEGPALyEDPPDQKtsPsGKPAtLKIC |
| P27797 | Y109 | Sugiyama | CALR CRTC | QTLVVQFTVKHEQNIDCGGGyVKLFPNSLDQTDMHGDSEYN |
| P28062 | Y271 | Sugiyama | PSMB8 LMP7 PSMB5i RING10 Y2 | MKEDGWVKVEsTDVSDLLHQyREANQ_______________ |
| P28066 | Y8 | Sugiyama | PSMA5 | _____________MFLTRsEyDRGVNtFsPEGRLFQVEyAI |
| P28074 | Y171 | Sugiyama | PSMB5 LMPX MB1 X | GMGLSMGTMICGWDKRGPGLyyVDsEGNRISGATFSVGSGS |
| P28074 | Y228 | Sugiyama | PSMB5 LMPX MB1 X | VEQAyDLARRAIyQATYRDAysGGAVNLyHVREDGWIRVSs |
| P28074 | Y236 | Sugiyama | PSMB5 LMPX MB1 X | RRAIyQATYRDAysGGAVNLyHVREDGWIRVSsDNVADLHE |
| P29144 | Y1042 | Sugiyama | TPP2 | TEALRDLKIQWMTKLDSsDIyNELKEtyPNyLPLyVARLHQ |
| P29350 | Y536 | EPSD|PSP | PTPN6 HCP PTP1C | IETTKKKLEVLQSQKGQEsEyGNITyPPAMKNAHAKAsRts |
| P29350 | Y564 | GPS6|SIGNOR|iPTMNet|EPSD|PSP | PTPN6 HCP PTP1C | AMKNAHAKAsRtssKHKEDVyENLHTKNKREEKVKKQRSAD |
| P29353 | Y427 | Sugiyama | SHC1 SHC SHCA | RKQMPPPPPCPGRELFDDPsyVNVQNLDKARQAVGGAGPPN |
| P29401 | S308 | Sugiyama | TKT | PPQEDAPsVDIANIRMPsLPsyKVGDKIATRKAYGQALAKL |
| P29401 | Y202 | Sugiyama | TKT | LDINRLGQsDPAPLQHQMDIyQKRCEAFGWHAIIVDGHSVE |
| P29401 | Y481 | Sugiyama | TKT | AANTKGICFIRTsRPENAIIyNNNEDFQVGQAKVVLKSKDD |
| P29692 | Y26 | Sugiyama | EEF1D EF1D | LAHEKIWFDKFKYDDAERRFyEQMNGPVAGAsRQENGAsVI |
| P30041 | Y89 | Sugiyama | PRDX6 AOP2 KIAA0106 | IALSIDSVEDHLAWSKDINAyNCEEPtEKLPFPIIDDRNRE |
| P30043 | S202 | Sugiyama | BLVRB FLR SCAN | GHFMLRCLttDEyDGHstyPsHQyQ________________ |
| P30043 | Y200 | Sugiyama | BLVRB FLR SCAN | DLGHFMLRCLttDEyDGHstyPsHQyQ______________ |
| P30043 | Y205 | Sugiyama | BLVRB FLR SCAN | MLRCLttDEyDGHstyPsHQyQ___________________ |
| P30085 | Y49 | Sugiyama | CMPK1 CMK CMPK UCK UMK UMPK | ytHLSAGELLRDERKNPDsQyGELIEKYIKEGKIVPVEITI |
| P30086 | T167 | Sugiyama | PEBP1 PBP PEBP | GKFKVAsFRKKyELRAPVAGtCyQAEWDDyVPKLyEQLsGK |
| P30086 | Y176 | Sugiyama | PEBP1 PBP PEBP | KKyELRAPVAGtCyQAEWDDyVPKLyEQLsGK_________ |
| P30086 | Y64 | Sugiyama | PEBP1 PBP PEBP | tQVKNRPtsIsWDGLDsGKLytLVLtDPDAPsRKDPKYREW |
| P30101 | Y100 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | LAKVDCTANTNTCNKyGVsGyPtLKIFRDGEEAGAyDGPRt |
| P30101 | Y115 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | yGVsGyPtLKIFRDGEEAGAyDGPRtADGIVsHLKKQAGPA |
| P30101 | Y356 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | FVMQEEFsRDGKALERFLQDyFDGNLKRyLKsEPIPESNDG |
| P30101 | Y445 | SIGNOR|Sugiyama | PDIA3 ERP57 ERP60 GRP58 | KDPNIVIAKMDAtANDVPsPyEVRGFPtIyFsPANKKLNPK |
| P30101 | Y454 | SIGNOR | PDIA3 ERP57 ERP60 GRP58 | MDAtANDVPsPyEVRGFPtIyFsPANKKLNPKKyEGGRELs |
| P30101 | Y467 | SIGNOR | PDIA3 ERP57 ERP60 GRP58 | VRGFPtIyFsPANKKLNPKKyEGGRELsDFIsyLQREAtNP |
| P30101 | Y67 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | LMLVEFFAPWCGHCKRLAPEyEAAAtRLKGIVPLAKVDCTA |
| P30101 | Y95 | Sugiyama | PDIA3 ERP57 ERP60 GRP58 | KGIVPLAKVDCTANTNTCNKyGVsGyPtLKIFRDGEEAGAy |
| P30419 | Y117 | GPS6|ELM|iPTMNet|EPSD | NMT1 NMT | ELFsVGQGPAKTMEEASKRSyQFWDtQPVPKLGEVVNtHGP |
| P30419 | Y180 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | NMT1 NMT | ALDLGDRGVLKELytLLNENyVEDDDNMFRFDYSPEFLLWA |
| P30622 | Y269 | Sugiyama | CLIP1 CYLN1 RSN | PLGKNDGAVAGtRyFQCQPKyGLFAPVHKVTKIGFPsttPA |
| P31153 | Y242 | Sugiyama | MAT2A AMS2 MATA2 | LKEKVIKAVVPAKyLDEDtIyHLQPsGRFVIGGPQGDAGLt |
| P31327 | Y1450 | Sugiyama | CPS1 | GsIDLVINLPNNNTKFVHDNyVIRRTAVDSGIPLLTNFQVT |
| P31327 | Y162 | Sugiyama | CPS1 | HWLATKsLGQWLQEEKVPAIyGVDtRMLTKIIRDKGTMLGK |
| P31327 | Y852 | Sugiyama | CPS1 | EWPsNLDLRKELSEPSsTRIyAIAKAIDDNMsLDEIEKLTY |
| P31689 | Y52 | Sugiyama | DNAJA1 DNAJ2 HDJ2 HSJ2 HSPF4 | KYHPDKNPNEGEKFKQISQAyEVLSDAKKRELYDKGGEQAI |
| P31939 | Y290 | Sugiyama | ATIC PURH OK/SW-cl.86 | PAGAAVGIPLsEDEAKVCMVyDLyKTLtPIsAAyARARGAD |
| P31939 | Y293 | Sugiyama | ATIC PURH OK/SW-cl.86 | AAVGIPLsEDEAKVCMVyDLyKTLtPIsAAyARARGADRMs |
| P31943 | Y266 | Sugiyama | HNRNPH1 HNRPH HNRPH1 | yNGYNDGYGFGSDRFGRDLNyCFsGMsDHRyGDGGstFQst |
| P31946 | Y106 | Sugiyama | YWHAB | EKIEAELQDICNDVLELLDKyLIPNATQPESKVFyLKMKGD |
| P31946 | Y151 | Sugiyama | YWHAB | LsEVAsGDNKQTtVsNsQQAyQEAFEIsKKEMQPTHPIRLG |
| P31946 | Y21 | Sugiyama | YWHAB | MTMDKsELVQKAKLAEQAERyDDMAAAMKAVtEQGHELsNE |
| P31946 | Y213 | Sugiyama | YWHAB | LAKTAFDEAIAELDtLNEEsyKDstLIMQLLRDNLtLWtSE |
| P31946 | Y50 | Sugiyama | YWHAB | AVtEQGHELsNEERNLLsVAyKNVVGARRSsWRVIsSIEQK |
| P31947 | Y151 | Sugiyama | SFN HME1 | LAEVATGDDKKRIIDSARsAyQEAMDISKKEMPPTNPIRLG |
| P31947 | Y48 | Sugiyama | SFN HME1 | GAVEKGEELsCEERNLLsVAyKNVVGGQRAAWRVLSsIEQK |
| P31948 | Y323 | Sugiyama | STIP1 | YARIGNSyFKEEKYKDAIHFyNKSLAEHRtPDVLKKCQQAE |
| P31948 | Y354 | Sugiyama | STIP1 | DVLKKCQQAEKILKEQERLAyINPDLALEEKNKGNECFQKG |
| P31948 | Y41 | Sugiyama | STIP1 | DDALQCysEAIKLDPHNHVLysNRsAAyAKKGDYQKAyEDG |
| P31994 | Y292 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | FCGR2B CD32 FCG2 IGFR2 | PANPTNPDEADKVGAENTITySLLMHPDALEEPDDQNRI__ |
| P31995 | Y310 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | FCGR2C CD32 FCG2 IGFR2 | ADGGyMTLNPRAPTDDDKNIyLTLPPNDHVNSNN_______ |
| P32119 | Y115 | Sugiyama | PRDX2 NKEFB TDPX1 | GLGPLNIPLLADVTRRLsEDyGVLKTDEGIAYRGLFIIDGK |
| P32927 | Y466 | EPSD|PSP | CSF2RB IL3RB IL5RB | ALIVIFLTIAVLLALRFCGIyGyRLRRKWEEKIPNPSKSHL |
| P32927 | Y468 | EPSD|PSP | CSF2RB IL3RB IL5RB | IVIFLTIAVLLALRFCGIyGyRLRRKWEEKIPNPSKSHLFQ |
| P32927 | Y822 | EPSD|PSP | CSF2RB IL3RB IL5RB | DVSPTSPQPEGLLVLQQVGDyCFLPGLGPGPLSLRSKPSSP |
| P32927 | Y882 | EPSD|PSP | CSF2RB IL3RB IL5RB | GQAVPQVPVIQLFKALKQQDyLSLPPWEVNKPGEVC_____ |
| P32929 | S61 | Sugiyama | CTH | ISLSTTFKQGAPGQHsGFEysRsGNPTRNCLEKAVAALDGA |
| P32929 | Y114 | Sugiyama | CTH | TVTITHLLKAGDQIICMDDVyGGTNRYFRQVASEFGLKISF |
| P32929 | Y60 | Sugiyama | CTH | PISLSTTFKQGAPGQHsGFEysRsGNPTRNCLEKAVAALDG |
| P32969 | Y180 | Sugiyama | RPL9 OK/SW-cl.103; RPL9P7; RPL9P8; RPL9P9 | LIQQATTVKNKDIRKFLDGIyVsEKGtVQQADE________ |
| P33121 | Y693 | Sugiyama | ACSL1 FACL1 FACL2 LACS LACS1 LACS2 | TMKAKRPELRNYFRSQIDDLyStIKV_______________ |
| P33316 | Y167 | Sugiyama | DUT | PPMEKAVVKTDIQIALPsGCyGRVAPRSGLAAKHFIDVGAG |
| P33778 | Y41 | Sugiyama | H2BC3 H2BFF HIST1H2BB | KAQKKDGKKRKRsRKEsysIyVyKVLKQVHPDTGISSKAMG |
| P33778 | Y43 | Sugiyama | H2BC3 H2BFF HIST1H2BB | QKKDGKKRKRsRKEsysIyVyKVLKQVHPDTGISSKAMGIM |
| P33993 | Y333 | Sugiyama | MCM7 CDC47 MCM2 | EsGAGELtREELRQIAEEDFyEKLAASIAPEIYGHEDVKKA |
| P33993 | Y600 | EPSD|PSP | MCM7 CDC47 MCM2 | YItAAYVEMRREAWASKDATyTSARTLLAILRLSTALARLR |
| P34931 | T47 | Sugiyama | HSPA1L | KVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVAMNPQN |
| P34931 | Y43 | Sugiyama | HSPA1L | FQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVAM |
| P34932 | Y30 | Sugiyama | HSPA4 APG2 HSPH2 | FQSCYVAVARAGGIETIANEysDRCtPACIsFGPKNRSIGA |
| P34932 | Y336 | Sugiyama | HSPA4 APG2 HSPH2 | RVEPPLRSVLEQTKLKKEDIyAVEIVGGATRIPAVKEKISK |
| P34932 | Y597 | Sugiyama | HSPA4 APG2 HSPH2 | VDLPIENQLLWQIDREMLNLyIENEGKMIMQDKLEKERNDA |
| P34932 | Y624 | Sugiyama | HSPA4 APG2 HSPH2 | MIMQDKLEKERNDAKNAVEEyVyEMRDKLSGEYEKFVSEDD |
| P34932 | Y626 | Sugiyama | HSPA4 APG2 HSPH2 | MQDKLEKERNDAKNAVEEyVyEMRDKLSGEYEKFVSEDDRN |
| P34932 | Y660 | Sugiyama | HSPA4 APG2 HSPH2 | VSEDDRNsFtLKLEDTENWLyEDGEDQPKQVYVDKLAELKN |
| P35221 | Y619 | Sugiyama | CTNNA1 | SSDPAQPMDENEFIDASRLVyDGIRDIRKAVLMIRtPEELD |
| P35270 | Y259 | Sugiyama | SPR | QKLLSLLEKDEFKSGAHVDFyDK__________________ |
| P35354 | Y120 | SIGNOR|EPSD|PSP | PTGS2 COX2 | SYVLTSRSHLIDSPPTYNADyGYKSWEAFSNLSYYTRALPP |
| P35579 | Y297 | Sugiyama | MYH9 | FYYLLSGAGEHLKTDLLLEPyNKyRFLsNGHVtIPGQQDKD |
| P35579 | Y754 | Sugiyama | MYH9 | MDGKQACVLMIKALELDsNLyRIGQSKVFFRAGVLAHLEEE |
| P35609 | Y385 | Sugiyama | ACTN2 | GKMVSDIAGAWQRLEQAEKGyEEWLLNEIRRLERLEHLAEK |
| P35637 | Y468 | Sugiyama | FUS TLS | KAPKPDGPGGGPGGsHMGGNyGDDRRGGRGGYDRGGYRGRG |
| P36873 | Y134 | Sugiyama | PPP1CC | YPENFFLLRGNHECAsINRIyGFyDECKRRYNIKLWKTFTD |
| P36873 | Y137 | Sugiyama | PPP1CC | NFFLLRGNHECAsINRIyGFyDECKRRYNIKLWKTFTDCFN |
| P37108 | Y27 | Sugiyama | SRP14 | EQFLtELTRLFQKCRTSGsVyItLKKYDGRTKPIPKKGtVE |
| P37802 | Y192 | Sugiyama | TAGLN2 KIAA0120 CDABP0035 | NVIGLQMGtNRGAsQAGMtGyGMPRQIL_____________ |
| P37837 | Y206 | Sugiyama | TALDO1 TAL TALDO TALDOR | ISPFVGRILDWHVANTDKKSyEPLEDPGVKSVTKIYNYYKK |
| P37840 | Y125 | iPTMNet|EPSD | SNCA NACP PARK1 | EGAPQEGILEDMPVDPDNEAyEMPsEEGyQDyEPEA_____ |
| P38646 | T120 | Sugiyama | HSPA9 GRP75 HSPA9B mt-HSP70 | LVGMPAKRQAVtNPNNtFyAtKRLIGRRYDDPEVQKDIKNV |
| P38646 | Y118 | Sugiyama | HSPA9 GRP75 HSPA9B mt-HSP70 | ERLVGMPAKRQAVtNPNNtFyAtKRLIGRRYDDPEVQKDIK |
| P38646 | Y196 | Sugiyama | HSPA9 GRP75 HSPA9B mt-HSP70 | EtAENyLGHtAKNAVItVPAyFNDsQRQAtKDAGQIsGLNV |
| P38646 | Y652 | Sugiyama | HSPA9 GRP75 HSPA9B mt-HSP70 | NIRQAAssLQQASLKLFEMAyKKMAsEREGSGsSGTGEQKE |
| P39019 | Y48 | Sugiyama | RPS19 | LKVPEWVDtVKLAKHKELAPyDENWFytRAAstARHLYLRG |
| P39019 | Y54 | Sugiyama | RPS19 | VDtVKLAKHKELAPyDENWFytRAAstARHLYLRGGAGVGs |
| P40259 | Y196 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | CD79B B29 IGB | PIFLLLDKDDSKAGMEEDHtyEGLDIDQTAtyEDIVTLRTG |
| P40259 | Y207 | GPS6|ELM|iPTMNet|EPSD | CD79B B29 IGB | KAGMEEDHtyEGLDIDQTAtyEDIVTLRTGEVKWsVGEHPG |
| P40261 | Y11 | Sugiyama | NNMT | __________MESGFTSKDTyLSHFNPRDYLEKYYKFGSRH |
| P40925 | Y210 | Sugiyama | MDH1 MDHA | tQYPDVNHAKVKLQGKEVGVyEALKDDsWLKGEFVttVQQR |
| P40939 | Y637 | Sugiyama | HADHA HADH | ELLTQMVSKGFLGRKSGKGFyIyQEGVKRKDLNSDMDSILA |
| P40939 | Y639 | Sugiyama | HADHA HADH | LTQMVSKGFLGRKSGKGFyIyQEGVKRKDLNSDMDSILASL |
| P41219 | Y287 | Sugiyama | PRPH NEF4 PRPH1 | DIRAQYESIAAKNLQEAEEWyKSKYADLSDAANRNHEALRQ |
| P41567 | Y30 | Sugiyama | EIF1 SUI1 | FDPFADAsKGDDLLPAGTEDyIHIRIQQRNGRKtLttVQGI |
| P42025 | Y33 | Sugiyama | ACTR1B CTRN2 | VIDNGSGVIKAGFAGDQIPKyCFPNyVGRPKHMRVMAGALE |
| P42025 | Y38 | Sugiyama | ACTR1B CTRN2 | SGVIKAGFAGDQIPKyCFPNyVGRPKHMRVMAGALEGDLFI |
| P42166 | Y127 | Sugiyama | TMPO LAP2 | KDDLDVtELTNEDLLDQLVKyGVNPGPIVGttRKLYEKKLL |
| P42167 | Y127 | Sugiyama | TMPO LAP2 | KDDLDVTELTNEDLLDQLVKyGVNPGPIVGtTRKLYEKKLL |
| P42224 | Y170 | Sugiyama | STAT1 | KDKVMCIEHEIKsLEDLQDEyDFKCKTLQNREHETNGVAKS |
| P42229 | Y694 | GPS6|ELM|iPTMNet|EPSD | STAT5A STAT5 | PKDEVFSKYYTPVLAKAVDGyVKPQIKQVVPEFVNASADAG |
| P42680 | Y519 | GPS6 | TEC PSCTK4 | EAGVVKVSDFGMARyVLDDQytsSsGAKFPVKWCPPEVFNY |
| P42684 | Y116 | GPS6 | ABL2 ABLL ARG | ssKENLLGATESDPNLFVALyDFVAsGDNTLSITKGEKLRV |
| P42684 | Y161 | GPS6 | ABL2 ABLL ARG | QNGEWsEVRSKNGQGWVPSNyITPVNSLEKHSWyHGPVSRS |
| P42684 | Y174 | GPS6 | ABL2 ABLL ARG | QGWVPSNyITPVNSLEKHSWyHGPVSRSAAEyLLSSLINGS |
| P42684 | Y185 | GPS6 | ABL2 ABLL ARG | VNSLEKHSWyHGPVSRSAAEyLLSSLINGSFLVREsEssPG |
| P42684 | Y218 | GPS6 | ABL2 ABLL ARG | REsEssPGQLsISLRYEGRVyHYRINTTADGKVyVTAESRF |
| P42684 | Y231 | GPS6 | ABL2 ABLL ARG | LRYEGRVyHYRINTTADGKVyVTAESRFSTLAELVHHHSTV |
| P42684 | Y261 | GPS6 | ABL2 ABLL ARG | LAELVHHHSTVADGLVTTLHyPAPKCNKPTVyGVsPIHDKW |
| P42768 | Y291 | SIGNOR|EPSD|PSP | WAS IMD2 | FSRAGIsEAQLtDAETsKLIyDFIEDQGGLEAVRQEMRRQE |
| P43034 | Y28 | Sugiyama | PAFAH1B1 LIS1 MDCR MDS PAFAHA | RDELNRAIADyLRSNGyEEAySVFKKEAELDVNEELDKKYA |
| P43405 | Y131 | EPSD | SYK | QGVQPKTGPFEDLKENLIREyVKQTWNLQGQALEQAIISQK |
| P43405 | Y323 | GPS6|EPSD|PSP | SYK | HRKssPAQGNRQEstVsFNPyEPELAPWAADKGPQREALPM |
| P43405 | Y348 | PSP | SYK | APWAADKGPQREALPMDtEVyEsPyADPEEIRPKEVYLDRK |
| P43405 | Y352 | PSP | SYK | ADKGPQREALPMDtEVyEsPyADPEEIRPKEVYLDRKLLTL |
| P43405 | Y525 | PSP | SYK | QHyAKISDFGLSKALRADENyyKAQTHGKWPVKWyAPECIN |
| P43405 | Y526 | PSP | SYK | HyAKISDFGLSKALRADENyyKAQTHGKWPVKWyAPECINy |
| P43490 | Y34 | Sugiyama | NAMPT PBEF PBEF1 | ATDSYKVTHYKQYPPNTSKVysyFECREKKTENSKLRKVKY |
| P43490 | Y36 | Sugiyama | NAMPT PBEF PBEF1 | DSYKVTHYKQYPPNTSKVysyFECREKKTENSKLRKVKYEE |
| P46527 | Y88 | GPS6|SIGNOR|iPTMNet|EPSD|PSP | CDKN1B KIP1 p27 | KPLEGKyEWQEVEKGsLPEFyyRPPRPPKGACKVPAQEsQD |
| P46777 | Y207 | Sugiyama | RPL5 MSTP030 | sKEFNAEVHRKHIMGQNVADyMRyLMEEDEDAyKKQFsQyI |
| P46777 | Y210 | Sugiyama | RPL5 MSTP030 | FNAEVHRKHIMGQNVADyMRyLMEEDEDAyKKQFsQyIKNs |
| P46777 | Y219 | Sugiyama | RPL5 MSTP030 | IMGQNVADyMRyLMEEDEDAyKKQFsQyIKNsVtPDMMEEM |
| P46777 | Y240 | Sugiyama | RPL5 MSTP030 | KKQFsQyIKNsVtPDMMEEMyKKAHAAIRENPVyEKKPKKE |
| P46778 | Y156 | Sugiyama | RPL21 | REAHFVRTNGKEPELLEPIPyEFMA________________ |
| P46778 | Y30 | Sugiyama | RPL21 | GTRYMFSRPFRKHGVVPLAtyMRIYKKGDIVDIKGMGTVQK |
| P46940 | Y140 | Sugiyama | IQGAP1 KIAA0051 | LNAMDEIGLPKIFYPETTDIyDRKNMPRCIYCIHALSLYLF |
| P46940 | Y1478 | Sugiyama | IQGAP1 KIAA0051 | KIQTGLKKLTELGtVDPKNKyQELINDIARDIRNQRRYRQR |
| P46940 | Y41 | Sugiyama | IQGAP1 KIAA0051 | LDNERLTAEEMDERRRQNVAyEyLCHLEEAKRWMEACLGED |
| P47224 | Y114 | Sugiyama | RABIF MSS4 RASGRF3 | CADCEIGPIGWHCLDDKNSFyVALERVSHE___________ |
| P47712 | Y535 | Sugiyama | PLA2G4A CPLA2 PLA2G4 | sFDDDELDAAVADPDEFERIyEPLDVKSKKIHVVDSGLTFN |
| P47756 | Y232 | Sugiyama | CAPZB | NIGRLVEDMENKIRstLNEIyFGKTKDIVNGLRSVQTFADK |
| P47813 | Y106 | Sugiyama | EIF1AX EIF1A EIF4C | DNKADVILKYNADEARsLKAyGELPEHAKINETDTFGPGDD |
| P47914 | Y98 | Sugiyama | RPL29 | PKEVKPKIPKGVSRKLDRLAyIAHPKLGKRARARIAKGLRL |
| P48637 | Y375 | Sugiyama | GSS | LAAPSRFVLKPQREGGGNNLyGEEMVQALKQLKDSEERAsy |
| P48643 | Y274 | Sugiyama | CCT5 CCTE KIAA0098 | PFEPPKPKTKHKLDVtsVEDyKALQKYEKEKFEEMIQQIKE |
| P48741 | T47 | Sugiyama | HSPA7 HSP70B | RVEILANDQGNRTtPsyVAFtDtERLVGDAAKsQAALNPHN |
| P48741 | Y43 | Sugiyama | HSPA7 HSP70B | FQQGRVEILANDQGNRTtPsyVAFtDtERLVGDAAKsQAAL |
| P49023 | Y88 | Sugiyama | PXN | QWQPSSSRFIHQQPQsssPVyGssAKtssVsNPQDsVGsPC |
| P49207 | Y32 | Sugiyama | RPL34 | sYNtASNKTRLSRTPGNRIVyLytKKVGKAPKSACGVCPGR |
| P49207 | Y34 | Sugiyama | RPL34 | NtASNKTRLSRTPGNRIVyLytKKVGKAPKSACGVCPGRLR |
| P49321 | Y540 | Sugiyama | NASP | DMLDLAKIIFKRQETKEAQLyAAQAHLKLGEVSVESENYVQ |
| P49327 | Y2454 | Sugiyama | FASN FAS | tPKAKyHGNVMLLRAKtGGAyGEDLGADyNLsQVCDGKVsV |
| P49327 | Y2462 | Sugiyama | FASN FAS | NVMLLRAKtGGAyGEDLGADyNLsQVCDGKVsVHVIEGDHR |
| P49327 | Y277 | Sugiyama | FASN FAS | KEQGVtFPsGDIQEQLIRSLyQsAGVAPEsFEyIEAHGtGT |
| P49327 | Y289 | Sugiyama | FASN FAS | QEQLIRSLyQsAGVAPEsFEyIEAHGtGTKVGDPQELNGIt |
| P49327 | Y45 | Sugiyama | FASN FAS | NLIGGVDMVTDDDRRWKAGLyGLPRRsGKLKDLSRFDAsFF |
| P49419 | Y55 | Sugiyama | ALDH7A1 ATQ1 | NQPQYAWLKELGLREENEGVyNGSWGGRGEVIttyCPANNE |
| P49588 | Y192 | Sugiyama | AARS1 AARS | KDNFWEMGDtGPCGPCsEIHyDRIGGRDAAHLVNQDDPNVL |
| P49588 | Y667 | Sugiyama | AARS1 AARS | QQIKKAEEIANEMIEAAKAVyTQDCPLAAAKAIQGLRAVFD |
| P49588 | Y690 | Sugiyama | AARS1 AARS | DCPLAAAKAIQGLRAVFDEtyPDPVRVVSIGVPVSELLDDP |
| P49591 | Y248 | Sugiyama | SARS1 SARS SERS | FMRKEVMQEVAQLsQFDEELyKVIGKGSEKSDDNSYDEKYL |
| P50395 | T408 | Sugiyama | GDI2 RABGDIB | VPKDLGtEsQIFIsRTyDAttHFEttCDDIKNIYKRMtGsE |
| P50395 | Y203 | Sugiyama | GDI2 RABGDIB | DFTGHALALYRtDDyLDQPCyEtINRIKLYsEsLARYGKsP |
| P50395 | Y404 | Sugiyama | GDI2 RABGDIB | SDLLVPKDLGtEsQIFIsRTyDAttHFEttCDDIKNIYKRM |
| P50402 | Y95 | Sugiyama | EMD EDMD STA | DLPKKEDALLyQsKGyNDDyyEEsyFTTRTyGEPEsAGPSR |
| P50454 | Y135 | Sugiyama | SERPINH1 CBP1 CBP2 HSP47 SERPINH2 PIG14 | LRSLSNSTARNVTWKLGsRLyGPssVsFADDFVRssKQHYN |
| P50502 | Y185 | Sugiyama | ST13 AAG2 FAM10A1 HIP SNC6 | NAAIRDCDRAIEINPDsAQPyKWRGKAHRLLGHWEEAAHDL |
| P50897 | Y264 | Sugiyama | PPT1 CLN1 PPT | FGFYRsGQAKEtIPLQEtsLytQDRLGLKEMDNAGQLVFLA |
| P50990 | Y30 | Sugiyama | CCT8 C21orf112 CCTQ KIAA0002 | GFAQMLKEGAKHFsGLEEAVyRNIQACKELAQTTRTAYGPN |
| P50990 | Y426 | Sugiyama | CCT8 C21orf112 CCTQ KIAA0002 | KRLVPGGGAtEIELAKQItsyGETCPGLEQyAIKKFAEAFE |
| P50990 | Y436 | Sugiyama | CCT8 C21orf112 CCTQ KIAA0002 | EIELAKQItsyGETCPGLEQyAIKKFAEAFEAIPRALAENS |
| P50991 | Y24 | Sugiyama | CCT4 CCTD SRB | NVAPRsGATAGAAGGRGKGAyQDRDKPAQIRFsNISAAKAV |
| P50991 | Y269 | Sugiyama | CCT4 CCTD SRB | IQFCLSAPKTDMDNQIVVSDyAQMDRVLREERAYILNLVKQ |
| P50995 | Y365 | Sugiyama | ANXA11 ANX11 | NRDESTNVDMSLAQRDAQELyAAGENRLGTDESKFNAVLCS |
| P50995 | Y482 | Sugiyama | ANXA11 ANX11 | sEtDLLDIRSEYKRMYGKsLyHDISGDtsGDyRKILLKICG |
| P50995 | Y493 | Sugiyama | ANXA11 ANX11 | YKRMYGKsLyHDISGDtsGDyRKILLKICGGND________ |
| P51116 | Y614 | Sugiyama | FXR2 FMR1L2 | RGNRtDGsIsGDRQPVtVADyIsRAEsQsRQRPPLERTKPs |
| P51812 | Y707 | Sugiyama | RPS6KA3 ISPK1 MAPKAPK1B RSK2 | QYQLNRQDAPHLVKGAMAAtysALNRNQsPVLEPVGRsTLA |
| P51965 | Y77 | Sugiyama | UBE2E1 UBCH6 | ADITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| P51991 | S375 | Sugiyama | HNRNPA3 HNRPA3 | ssGsPyGGGyGsGGGsGGyGsRRF_________________ |
| P52272 | Y681 | Sugiyama | HNRNPM HNRPM NAGR1 | PFDFTWKMLKDKFNECGHVLyADIKMENGKSKGCGVVKFEs |
| P52565 | Y156 | Sugiyama | ARHGDIA GDIA1 | GVKIDKtDyMVGsYGPRAEEyEFLtPVEEAPKGMLARGsYs |
| P52788 | Y336 | Sugiyama | SMS | GNCVNLTEALSLYEEQLGRLyCPVEFSKEIVCVPSYLELWV |
| P52907 | Y239 | Sugiyama | CAPZA1 | sNEAQtAKEFIKIIENAENEyQTAIsENyQtMSDTTFKALR |
| P52907 | Y247 | Sugiyama | CAPZA1 | EFIKIIENAENEyQTAIsENyQtMSDTTFKALRRQLPVTRT |
| P52948 | Y1215 | Sugiyama | NUP98 ADAR2 | KVHLEKLSLRQRKPDEDMKLyQTPLELKLKHSTVHVDELCP |
| P52948 | Y208 | Sugiyama | NUP98 ADAR2 | CITAMKEYESKSLEELRLEDyQANRKGPQNQVGAGTTTGLF |
| P52948 | Y627 | Sugiyama | NUP98 ADAR2 | NsNLFsPVNRDsENLAsPsEyPENGERFsFLSKPVDENHQQ |
| P52948 | Y848 | Sugiyama | NUP98 ADAR2 | PTDKTSRCLIKsPDRLADINyEGRLEAVSRKQGAQFKEyRP |
| P53396 | Y131 | PSP | ACLY | VPHSQAEEFYVCIYATREGDyVLFHHEGGVDVGDVDAKAQK |
| P53396 | Y227 | GPS6|SIGNOR|PSP | ACLY | VTKDGVyVLDLAAKVDATADyICKVKWGDIEFPPPFGREAy |
| P53396 | Y252 | GPS6|SIGNOR|PSP | ACLY | KWGDIEFPPPFGREAyPEEAyIADLDAKSGASLKLTLLNPK |
| P53396 | Y384 | PSP | ACLY | YQGPLKEHEVTIFVRRGGPNyQEGLRVMGEVGKTTGIPIHV |
| P53396 | Y652 | Sugiyama | ACLY | GCFKIGNTGGMLDNILASKLyRPGsVAyVSRsGGMsNELNN |
| P53396 | Y659 | PSP|Sugiyama | ACLY | TGGMLDNILASKLyRPGsVAyVSRsGGMsNELNNIISRTTD |
| P53396 | Y682 | GPS6|SIGNOR|PSP | ACLY | RsGGMsNELNNIISRTTDGVyEGVAIGGDRYPGSTFMDHVL |
| P53597 | Y78 | Sugiyama | SUCLG1 | IICQGFTGKQGtFHSQQALEyGtKLVGGTTPGKGGQTHLGL |
| P53621 | Y391 | Sugiyama | COPA | NPAENAVLLCTRAsNLENstyDLytIPKDADsQNPDAPEGK |
| P53621 | Y394 | Sugiyama | COPA | ENAVLLCTRAsNLENstyDLytIPKDADsQNPDAPEGKRSS |
| P53621 | Y733 | Sugiyama | COPA | LEKLRKMMKIAEIRKDMsGHyQNALyLGDVSERVRILKNCG |
| P53621 | Y738 | Sugiyama | COPA | KMMKIAEIRKDMsGHyQNALyLGDVSERVRILKNCGQKsLA |
| P53634 | Y438 | Sugiyama | CTSC CPPI | SGMDYWIVKNsWGtGWGENGyFRIRRGtDECAIEsIAVAAt |
| P53675 | Y921 | Sugiyama | CLTCL1 CLH22 CLTCL CLTD | DSSVVGRYCEKRDPHLACVAyERGQCDLELIKVCNENSLFK |
| P54105 | Y38 | Sugiyama | CLNS1A CLCI ICLN | RQQPDTEAVLNGKGLGtGtLyIAEsRLSWLDGsGLGFSLEY |
| P54577 | Y198 | Sugiyama | YARS1 YARS | KVDAQFGGIDQRKIFTFAEKyLPALGySKRVHLMNPMVPGL |
| P54577 | Y204 | Sugiyama | YARS1 YARS | GGIDQRKIFTFAEKyLPALGySKRVHLMNPMVPGLTGSKMS |
| P54577 | Y289 | Sugiyama | YARS1 YARS | FPLKSEFVILRDEKWGGNKTytAyVDLEKDFAAEVVHPGDL |
| P54577 | Y292 | Sugiyama | YARS1 YARS | KSEFVILRDEKWGGNKTytAyVDLEKDFAAEVVHPGDLKNS |
| P54577 | Y388 | Sugiyama | YARS1 YARS | LDIRVGKIITVEKHPDADsLyVEKIDVGEAEPRTVVSGLVQ |
| P54652 | T46 | Sugiyama | HSPA2 | KVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVAMNPTN |
| P54652 | Y42 | Sugiyama | HSPA2 | FQHGKVEIIANDQGNRttPsyVAFtDtERLIGDAAKNQVAM |
| P55060 | Y369 | Sugiyama | CSE1L CAS XPO2 | VPNMEFRAADEEAFEDNsEEyIRRDLEGsDIDTRRRAACDL |
| P55072 | Y495 | Sugiyama | VCP HEL-220 HEL-S-70 | TWEDIGGLEDVKRELQELVQyPVEHPDKFLKFGMtPSKGVL |
| P55084 | Y244 | Sugiyama | HADHB MSTP029 | GHSADRLAAAFAVSRLEQDEyALRsHSLAKKAQDEGLLSDV |
| P55209 | Y106 | Sugiyama | NAP1L1 NRP | VKCAQIEAKFyEEVHDLERKyAVLyQPLFDKRFEIINAIYE |
| P55209 | Y110 | Sugiyama | NAP1L1 NRP | QIEAKFyEEVHDLERKyAVLyQPLFDKRFEIINAIYEPTEE |
| P55795 | Y266 | Sugiyama | HNRNPH2 FTP3 HNRPH2 | YGGYNDGYGFGSDRFGRDLNyCFsGMsDHRyGDGGssFQst |
| P55884 | Y222 | Sugiyama | EIF3B EIF3S9 | KLKNVIHKIFSKFGKITNDFyPEEDGKTKGyIFLEyAsPAH |
| P57053 | Y41 | Sugiyama | H2BC12L H2BFS H2BS1 | KAQKKDGRKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| P57053 | Y43 | Sugiyama | H2BC12L H2BFS H2BS1 | QKKDGRKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| P58876 | Y41 | Sugiyama | H2BC5 H2BFB HIRIP2 HIST1H2BD | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| P58876 | Y43 | Sugiyama | H2BC5 H2BFB HIRIP2 HIST1H2BD | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| P60174 | S212 | Sugiyama | TPI1 TPI | WLKsNVsDAVAQstRIIyGGsVtGAtCKELASQPDVDGFLV |
| P60174 | Y209 | Sugiyama | TPI1 TPI | LRGWLKsNVsDAVAQstRIIyGGsVtGAtCKELASQPDVDG |
| P60174 | Y48 | Sugiyama | TPI1 TPI | tLNAAKVPADtEVVCAPPtAyIDFARQKLDPKIAVAAQNCy |
| P60174 | Y68 | Sugiyama | TPI1 TPI | yIDFARQKLDPKIAVAAQNCyKVTNGAFtGEIsPGMIKDCG |
| P60228 | Y445 | Sugiyama | EIF3E EIF3S6 INT6 | KLNQNSRSEAPNWAtQDsGFy____________________ |
| P60484 | Y240 | EPSD|PSP | PTEN MMAC1 TEP1 | LKVKIYSSNsGPtRREDKFMyFEFPQPLPVCGDIKVEFFHK |
| P60660 | S30 | Sugiyama | MYL6 | AEFKEAFQLFDRtGDGKILysQCGDVMRALGQNPtNAEVLK |
| P60660 | Y29 | Sugiyama | MYL6 | TAEFKEAFQLFDRtGDGKILysQCGDVMRALGQNPtNAEVL |
| P60660 | Y86 | Sugiyama | MYL6 | DFEHFLPMLQTVAKNKDQGtyEDyVEGLRVFDKEGNGtVMG |
| P60660 | Y89 | Sugiyama | MYL6 | HFLPMLQTVAKNKDQGtyEDyVEGLRVFDKEGNGtVMGAEI |
| P60709 | S239 | Sugiyama | ACTB | VALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPE |
| P60709 | Y198 | Sugiyama | ACTB | LDLAGRDLTDyLMKILtERGysFtttAEREIVRDIKEKLCy |
| P60709 | Y240 | Sugiyama | ACTB | ALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPEA |
| P60709 | Y306 | Sugiyama | ACTB | DVDIRKDLyANtVLsGGttMyPGIADRMQKEItALAPstMK |
| P60709 | Y362 | Sugiyama | ACTB | GGsILAsLstFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P60709 | Y91 | Sugiyama | ACTB | IEHGIVTNWDDMEKIWHHtFyNELRVAPEEHPVLLtEAPLN |
| P60842 | Y197 | Sugiyama | EIF4A1 DDX2A EIF4A | KMFVLDEADEMLsRGFKDQIyDIFQKLNsNtQVVLLSATMP |
| P60842 | Y70 | Sugiyama | EIF4A1 DDX2A EIF4A | yGFEKPsAIQQRAILPCIKGyDVIAQAQsGtGKTATFAISI |
| P60900 | Y160 | Sugiyama | PSMA6 PROS27 | LIGIDEEQGPQVYKCDPAGyyCGFKATAAGVKQtEstsFLE |
| P60981 | Y82 | Sugiyama | DSTN ACTDP DSN | VTITDPFKHFVGMLPEKDCRyALyDAsFETKESRKEELMFF |
| P60981 | Y85 | Sugiyama | DSTN ACTDP DSN | TDPFKHFVGMLPEKDCRyALyDAsFETKESRKEELMFFLWA |
| P61024 | Y7 | Sugiyama | CKS1B CKS1 PNAS-143 PNAS-16 | ______________MSHKQIyysDKyDDEEFEyRHVMLPKD |
| P61081 | T176 | Sugiyama | UBE2M UBC12 | NRRLFEQNVQRSMRGGyIGstyFERCLK_____________ |
| P61081 | Y172 | Sugiyama | UBE2M UBC12 | VLQNNRRLFEQNVQRSMRGGyIGstyFERCLK_________ |
| P61081 | Y177 | Sugiyama | UBE2M UBC12 | RRLFEQNVQRSMRGGyIGstyFERCLK______________ |
| P61158 | Y231 | Sugiyama | ACTR3 ARP3 | REVGIPPEQSLETAKAVKERysyVCPDLVKEFNKYDTDGSK |
| P61158 | Y233 | Sugiyama | ACTR3 ARP3 | VGIPPEQSLETAKAVKERysyVCPDLVKEFNKYDTDGSKWI |
| P61158 | Y400 | Sugiyama | ACTR3 ARP3 | GGSMLASTPEFYQVCHTKKDyEEIGPsICRHNPVFGVMs__ |
| P61163 | Y33 | Sugiyama | ACTR1A CTRN1 | VIDNGSGVIKAGFAGDQIPKyCFPNyVGRPKHVRVMAGALE |
| P61163 | Y38 | Sugiyama | ACTR1A CTRN1 | SGVIKAGFAGDQIPKyCFPNyVGRPKHVRVMAGALEGDIFI |
| P61247 | Y205 | Sugiyama | RPS3A FTE1 MFTL | VNKLIPDsIGKDIEKACQsIyPLHDVFVRKVKMLKKPKFEL |
| P61247 | Y256 | Sugiyama | RPS3A FTE1 MFTL | sssGKAtGDEtGAKVERADGyEPPVQEsV____________ |
| P61247 | Y31 | Sugiyama | RPS3A FTE1 MFTL | KGGKKGAKKKVVDPFSKKDWyDVKAPAMFNIRNIGKTLVTR |
| P61313 | Y6 | Sugiyama | RPL15 EC45 TCBAP0781 | _______________MGAYKyIQELWRKKQSDVMRFLLRVR |
| P61353 | S39 | Sugiyama | RPL27 | SGRKAVIVKNIDDGtsDRPysHALVAGIDRyPRKVTAAMGK |
| P61353 | Y75 | Sugiyama | RPL27 | AAMGKKKIAKRSKIKSFVKVyNyNHLMPtRysVDIPLDKtV |
| P61353 | Y77 | Sugiyama | RPL27 | MGKKKIAKRSKIKSFVKVyNyNHLMPtRysVDIPLDKtVVN |
| P61353 | Y85 | Sugiyama | RPL27 | RSKIKSFVKVyNyNHLMPtRysVDIPLDKtVVNKDVFRDPA |
| P61604 | T79 | Sugiyama | HSPE1 | EIQPVsVKVGDKVLLPEyGGtKVVLDDKDyFLFRDGDILGK |
| P61604 | Y76 | Sugiyama | HSPE1 | KGGEIQPVsVKVGDKVLLPEyGGtKVVLDDKDyFLFRDGDI |
| P61978 | Y323 | Sugiyama | HNRNPK HNRPK | RARNLPLPPPPPPRGGDLMAyDRRGRPGDRYDGMVGFSADE |
| P61978 | Y72 | Sugiyama | HNRNPK HNRPK | KNAGAVIGKGGKNIKALRtDyNAsVsVPDssGPERILsISA |
| P61981 | S215 | Sugiyama | YWHAG | HLAKtAFDDAIAELDtLNEDsyKDstLIMQLLRDNLtLWts |
| P61981 | Y20 | Sugiyama | YWHAG | _MVDREQLVQKARLAEQAERyDDMAAAMKNVtELNEPLsNE |
| P61981 | Y49 | Sugiyama | YWHAG | NVtELNEPLsNEERNLLsVAyKNVVGARRSsWRVIsSIEQK |
| P62081 | Y177 | Sugiyama | RPS7 | HLDKAQQNNVEHKVEtFsGVyKKLTGKDVNFEFPEFQL___ |
| P62136 | Y134 | Sugiyama | PPP1CA PPP1A | YPENFFLLRGNHECAsINRIyGFyDECKRRYNIKLWKTFTD |
| P62136 | Y137 | Sugiyama | PPP1CA PPP1A | NFFLLRGNHECAsINRIyGFyDECKRRYNIKLWKTFTDCFN |
| P62140 | Y133 | Sugiyama | PPP1CB | YPENFFLLRGNHECAsINRIyGFyDECKRRFNIKLWKTFTD |
| P62140 | Y136 | Sugiyama | PPP1CB | NFFLLRGNHECAsINRIyGFyDECKRRFNIKLWKTFTDCFN |
| P62140 | Y304 | Sugiyama | PPP1CB | VDETLMCSFQILKPSEKKAKyQyGGLNsGRPVtPPRTANPP |
| P62140 | Y306 | Sugiyama | PPP1CB | ETLMCSFQILKPSEKKAKyQyGGLNsGRPVtPPRTANPPKK |
| P62191 | Y225 | Sugiyama | PSMC1 | LTHPEyyEEMGIKPPKGVILyGPPGtGKTLLAKAVANQTsA |
| P62191 | Y439 | Sugiyama | PSMC1 | FKKSKENVLyKKQEGtPEGLyL___________________ |
| P62195 | Y148 | Sugiyama | PSMC5 SUG1 | PNKVDPLVSLMMVEKVPDSTyEMIGGLDKQIKEIKEVIELP |
| P62241 | Y113 | Sugiyama | RPS8 OK/SW-cl.83 | TKTLVKNCIVLIDStPYRQWyEsHyALPLGRKKGAKLtPEE |
| P62241 | Y117 | Sugiyama | RPS8 OK/SW-cl.83 | VKNCIVLIDStPYRQWyEsHyALPLGRKKGAKLtPEEEEIL |
| P62249 | Y115 | Sugiyama | RPS16 | YYQKYVDEASKKEIKDILIQyDRtLLVADPRRCESKKFGGP |
| P62258 | Y152 | Sugiyama | YWHAE | LAEFAtGNDRKEAAENsLVAyKAAsDIAMtELPPTHPIRLG |
| P62258 | Y20 | Sugiyama | YWHAE | _MDDREDLVyQAKLAEQAERyDEMVESMKKVAGMDVELTVE |
| P62258 | Y49 | Sugiyama | YWHAE | KVAGMDVELTVEERNLLsVAyKNVIGARRASWRIIssIEQK |
| P62263 | Y72 | Sugiyama | RPS14 PRO2640 | TICRVTGGMKVKADRDEssPyAAMLAAQDVAQRCKELGITA |
| P62269 | Y95 | Sugiyama | RPS18 D6S218E | RQYKIPDWFLNRQKDVKDGKysQVLANGLDNKLREDLERLK |
| P62273 | Y7 | Sugiyama | RPS29 | ______________MGHQQLyWsHPRKFGQGSRSCRVCSNR |
| P62280 | Y55 | Sugiyama | RPS11 | RYYKNIGLGFKtPKEAIEGtyIDKKCPFTGNVsIRGRILsG |
| P62312 | Y72 | Sugiyama | LSM6 | VNGQLKNKyGDAFIRGNNVLyIstQKRRM____________ |
| P62333 | Y328 | Sugiyama | PSMC6 SUG2 | ARLDILKIHAGPITKHGEIDyEAIVKLSDGFNGADLRNVCT |
| P62424 | Y230 | Sugiyama | RPL7A SURF-3 SURF3 | EDKGALAKLVEAIRTNyNDRyDEIRRHWGGNVLGPKSVARI |
| P62633 | Y120 | Sugiyama | CNBP RNF163 ZNF9 | NCGKPGHLARDCDHADEQKCysCGEFGHIQKDCTKVKCYRC |
| P62633 | Y75 | Sugiyama | CNBP RNF163 ZNF9 | YRCGESGHLAKDCDLQEDACyNCGRGGHIAKDCKEPKRERE |
| P62736 | S241 | Sugiyama | ACTA2 ACTSA ACTVS GIG46 | VALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPE |
| P62736 | Y242 | Sugiyama | ACTA2 ACTSA ACTVS GIG46 | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P62750 | Y117 | Sugiyama | RPL23A | VFIVDVKANKHQIKQAVKKLyDIDVAKVNtLIRPDGEKKAY |
| P62750 | Y144 | Sugiyama | RPL23A | VNtLIRPDGEKKAYVRLAPDyDALDVANKIGII________ |
| P62753 | Y156 | Sugiyama | RPS6 OK/SW-cl.2 | KRASRIRKLFNLsKEDDVRQyVVRKPLNKEGKKPRTKAPKI |
| P62805 | Y52 | Sugiyama | H4C1 H4/A H4FA HIST1H4A; H4C2 H4/I H4FI HIST1H4B; H4C3 H4/G H4FG HIST1H4C; H4C4 H4/B H4FB HIST1H4D; H4C5 H4/J H4FJ HIST1H4E; H4C6 H4/C H4FC HIST1H4F; H4C8 H4/H H4FH HIST1H4H; H4C9 H4/M H4FM HIST1H4I; H4C11 H4/E H4FE HIST1H4J; H4C12 H4/D H4FD HIST1H4K; H4C13 H4/K H4FK HIST1H4L; H4C14 H4/N H4F2 H4FN HIST2H4 HIST2H4A; H4C15 H4/O H4FO HIST2H4B; H4C16 H4-16 HIST4H4 | KPAIRRLARRGGVKRIsGLIyEETRGVLKVFLENVIRDAVt |
| P62807 | Y41 | Sugiyama | H2BC4 H2BFL HIST1H2BC; H2BC6 H2BFH HIST1H2BE; H2BC7 H2BFG HIST1H2BF; H2BC8 H2BFA HIST1H2BG; H2BC10 H2BFK HIST1H2BI | KAQKKDGKKRKRsRKEsysVyVyKVLKQVHPDTGIssKAMG |
| P62807 | Y43 | Sugiyama | H2BC4 H2BFL HIST1H2BC; H2BC6 H2BFH HIST1H2BE; H2BC7 H2BFG HIST1H2BF; H2BC8 H2BFA HIST1H2BG; H2BC10 H2BFK HIST1H2BI | QKKDGKKRKRsRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| P62826 | Y146 | Sugiyama | RAN ARA24 OK/SW-cl.81 | IKDRKVKAKsIVFHRKKNLQyyDIsAKSNyNFEKPFLWLAR |
| P62826 | Y147 | Sugiyama | RAN ARA24 OK/SW-cl.81 | KDRKVKAKsIVFHRKKNLQyyDIsAKSNyNFEKPFLWLARK |
| P62829 | Y38 | Sugiyama | RPL23 | LGLPVGAVINCADNTGAKNLyIIsVKGIKGRLNRLPAAGVG |
| P62847 | Y76 | Sugiyama | RPS24 | FVFGFRTHFGGGKttGFGMIyDsLDyAKKNEPKHRLARHGL |
| P62847 | Y81 | Sugiyama | RPS24 | RTHFGGGKttGFGMIyDsLDyAKKNEPKHRLARHGLYEKKK |
| P62888 | Y62 | Sugiyama | RPL30 | KAKLVILANNCPALRKsEIEyyAMLAKtGVHHysGNNIELG |
| P62888 | Y63 | Sugiyama | RPL30 | AKLVILANNCPALRKsEIEyyAMLAKtGVHHysGNNIELGt |
| P62899 | T26 | Sugiyama | RPL31 | KGGEKKKGRsAINEVVtREytINIHKRIHGVGFKKRAPRAL |
| P62899 | Y103 | Sugiyama | RPL31 | RIRVRLSRKRNEDEDsPNKLytLVtyVPVttFKNLQtVNVD |
| P62899 | Y108 | Sugiyama | RPL31 | LSRKRNEDEDsPNKLytLVtyVPVttFKNLQtVNVDEN___ |
| P62899 | Y25 | Sugiyama | RPL31 | KKGGEKKKGRsAINEVVtREytINIHKRIHGVGFKKRAPRA |
| P62906 | Y11 | Sugiyama | RPL10A NEDD6 | __________MSSKVsRDtLyEAVREVLHGNQRKRRKFLET |
| P62913 | Y170 | Sugiyama | RPL11 | CIGAKHRISKEEAMRWFQQKyDGIILPGK____________ |
| P62917 | S130 | Sugiyama | RPL8 | GTIVCCLEEKPGDRGKLARAsGNyAtVIsHNPEtKKtRVKL |
| P62917 | Y133 | Sugiyama | RPL8 | VCCLEEKPGDRGKLARAsGNyAtVIsHNPEtKKtRVKLPSG |
| P62937 | Y79 | Sugiyama | PPIA CYPA | GFMCQGGDFtRHNGTGGKsIyGEKFEDENFILKHtGPGILs |
| P62979 | Y148 | Sugiyama | RPS27A UBA80 UBCEP1 | AGVFMAsHFDRHyCGKCCLtyCFNKPEDK____________ |
| P63104 | Y149 | Sugiyama | YWHAZ | LAEVAAGDDKKGIVDQsQQAyQEAFEIsKKEMQPTHPIRLG |
| P63104 | Y211 | Sugiyama | YWHAZ | LAKtAFDEAIAELDtLsEEsyKDstLIMQLLRDNLtLWtsD |
| P63104 | Y48 | Sugiyama | YWHAZ | sVtEQGAELsNEERNLLsVAyKNVVGARRssWRVVssIEQK |
| P63220 | Y53 | Sugiyama | RPS21 | QMNVAEVDKVTGRFNGQFKtyAICGAIRRMGEsDDsILRLA |
| P63261 | S239 | Sugiyama | ACTG1 ACTG | VALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPE |
| P63261 | Y198 | Sugiyama | ACTG1 ACTG | LDLAGRDLTDyLMKILtERGysFtttAEREIVRDIKEKLCy |
| P63261 | Y240 | Sugiyama | ACTG1 ACTG | ALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPEA |
| P63261 | Y306 | Sugiyama | ACTG1 ACTG | DVDIRKDLyANtVLsGGttMyPGIADRMQKEItALAPstMK |
| P63261 | Y362 | Sugiyama | ACTG1 ACTG | GGsILAsLstFQQMWISKQEyDEsGPsIVHRKCF_______ |
| P63261 | Y91 | Sugiyama | ACTG1 ACTG | IEHGIVTNWDDMEKIWHHtFyNELRVAPEEHPVLLtEAPLN |
| P63267 | S240 | Sugiyama | ACTG2 ACTA3 ACTL3 ACTSG | VALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPE |
| P63267 | Y241 | Sugiyama | ACTG2 ACTA3 ACTL3 ACTSG | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P67809 | S209 | Sugiyama | YBX1 NSEP1 YB1 | RRRRFPPyyMRRPYGRRPQysNPPVQGEVMEGADNQGAGEQ |
| P67809 | Y196 | Sugiyama | YBX1 NSEP1 YB1 | sAPEGQAQQRRPyRRRRFPPyyMRRPYGRRPQysNPPVQGE |
| P67809 | Y197 | Sugiyama | YBX1 NSEP1 YB1 | APEGQAQQRRPyRRRRFPPyyMRRPYGRRPQysNPPVQGEV |
| P68032 | S241 | Sugiyama | ACTC1 ACTC | VALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPE |
| P68032 | Y242 | Sugiyama | ACTC1 ACTC | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P68032 | Y93 | Sugiyama | ACTC1 ACTC | IEHGIItNWDDMEKIWHHtFyNELRVAPEEHPtLLTEAPLN |
| P68104 | T88 | Sugiyama | EEF1A1 EEF1A EF1A LENG7 | ERGITIDISLWKFEtsKyyVtIIDAPGHRDFIKNMITGTSQ |
| P68104 | Y254 | Sugiyama | EEF1A1 EEF1A EF1A LENG7 | CILPPtRPTDKPLRLPLQDVyKIGGIGtVPVGRVEtGVLKP |
| P68104 | Y29 | Sugiyama | EEF1A1 EEF1A EF1A LENG7 | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| P68104 | Y85 | Sugiyama | EEF1A1 EEF1A EF1A LENG7 | AERERGITIDISLWKFEtsKyyVtIIDAPGHRDFIKNMITG |
| P68104 | Y86 | Sugiyama | EEF1A1 EEF1A EF1A LENG7 | ERERGITIDISLWKFEtsKyyVtIIDAPGHRDFIKNMITGT |
| P68133 | S241 | Sugiyama | ACTA1 ACTA | VALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPE |
| P68133 | Y242 | Sugiyama | ACTA1 ACTA | ALDFENEMAtAAssssLEKsyELPDGQVItIGNERFRCPET |
| P68133 | Y93 | Sugiyama | ACTA1 ACTA | IEHGIItNWDDMEKIWHHtFyNELRVAPEEHPtLLTEAPLN |
| P68363 | T225 | Sugiyama | TUBA1B | DNEAIYDICRRNLDIERPtytNLNRLIsQIVSsITASLRFD |
| P68363 | Y103 | Sugiyama | TUBA1B | yRQLFHPEQLItGKEDAANNyARGHYTIGKEIIDLVLDRIR |
| P68363 | Y432 | Sugiyama | TUBA1B | GMEEGEFSEAREDMAALEKDyEEVGVDsVEGEGEEEGEEy_ |
| P68363 | Y451 | Sugiyama | TUBA1B | DyEEVGVDsVEGEGEEEGEEy____________________ |
| P68366 | T225 | Sugiyama | TUBA4A TUBA1 | DNEAIYDICRRNLDIERPtytNLNRLIsQIVSsITASLRFD |
| P68366 | Y103 | Sugiyama | TUBA4A TUBA1 | YRQLFHPEQLItGKEDAANNyARGHYTIGKEIIDPVLDRIR |
| P68400 | Y255 | GPS6|ELM|iPTMNet|EPSD|Sugiyama | CSNK2A1 CK2A1 | GHDNYDQLVRIAKVLGTEDLyDyIDKYNIELDPRFNDILGR |
| P78316 | Y119 | Sugiyama | NOP14 C4orf9 NOL14 RES4-25 | EKMMKRFALEQQRHHEKKSIyNLNEDEELTHyGQsLADIEK |
| P78316 | Y130 | Sugiyama | NOP14 C4orf9 NOL14 RES4-25 | QRHHEKKSIyNLNEDEELTHyGQsLADIEKHNDIVDsDsDA |
| P78318 | Y277 | Sugiyama | IGBP1 IBP1 | AGYPSLPTMTVSDWYEQHRKyGALPDQGIAKAAPEEFRKAA |
| P78345 | Y29 | Sugiyama | RPP38 | GRGsLRKTRPLVVKTSLNNPyIIRWSALESEDMHFILQTLE |
| P83731 | Y11 | Sugiyama | RPL24 | __________MKVELCsFsGyKIYPGHGRRYARTDGKVFQF |
| P84103 | Y13 | Sugiyama | SRSF3 SFRS3 SRP20 | ________MHRDsCPLDCKVyVGNLGNNGNKtELERAFGyy |
| P84103 | Y33 | Sugiyama | SRSF3 SFRS3 SRP20 | yVGNLGNNGNKtELERAFGyyGPLRSVWVARNPPGFAFVEF |
| P98082 | Y38 | Sugiyama | DAB2 DOC2 | AAPKAPsKKEKKKGPEKTDEyLLARFKGDGVKYKAKLIGID |
| P98175 | Y694 | Sugiyama | RBM10 DXS8237E GPATC9 GPATCH9 KIAA0122 | QPISSLRDDERREsAtADAGyAILEKKGALAERQHTsMDLP |
| P98179 | Y118 | Sugiyama | RBM3 RNPL | GRGRSYSRGGGDQGYGSGRyyDsRPGGyGyGyGRSRDYNGR |
| P98179 | Y125 | Sugiyama | RBM3 RNPL | RGGGDQGYGSGRyyDsRPGGyGyGyGRSRDYNGRNQGGYDR |
| P98179 | Y127 | Sugiyama | RBM3 RNPL | GGDQGYGSGRyyDsRPGGyGyGyGRSRDYNGRNQGGYDRys |
| Q00059 | Y165 | Sugiyama | TFAM TCF6 TCF6L2 | KKKELTLLGKPKRPRsAYNVyVAERFQEAKGDsPQEKLKTV |
| Q00526 | Y15 | Sugiyama | CDK3 CDKN3 | ______MDMFQKVEKIGEGtyGVVyKAKNRETGQLVALKKI |
| Q00526 | Y19 | Sugiyama | CDK3 CDKN3 | __MDMFQKVEKIGEGtyGVVyKAKNRETGQLVALKKIRLDL |
| Q00534 | Y24 | Sugiyama | CDK6 CDKN6 | DGLCRADQQyECVAEIGEGAyGKVFKARDLKNGGRFVALKR |
| Q00610 | Y883 | Sugiyama | CLTC CLH17 CLTCL2 KIAA0034 | EARIHEGCEEPAtHNALAKIyIDsNNNPERFLRENPyyDsR |
| Q00610 | Y899 | Sugiyama | CLTC CLH17 CLTCL2 KIAA0034 | LAKIyIDsNNNPERFLRENPyyDsRVVGKYCEKRDPHLACV |
| Q00610 | Y900 | Sugiyama | CLTC CLH17 CLTCL2 KIAA0034 | AKIyIDsNNNPERFLRENPyyDsRVVGKYCEKRDPHLACVA |
| Q00610 | Y921 | Sugiyama | CLTC CLH17 CLTCL2 KIAA0034 | DsRVVGKYCEKRDPHLACVAyERGQCDLELINVCNENSLFK |
| Q00653 | Y247 | Sugiyama | NFKB2 LYT10 | NLKISRMDKTAGSVRGGDEVyLLCDKVQKDDIEVRFYEDDE |
| Q00839 | Y257 | Sugiyama | HNRNPU C1orf199 HNRPU SAFA U21.1 | QKGGDKKRGVKRPREDHGRGyFEyIEENKysRAKsPQPPVE |
| Q00839 | Y260 | Sugiyama | HNRNPU C1orf199 HNRPU SAFA U21.1 | GDKKRGVKRPREDHGRGyFEyIEENKysRAKsPQPPVEEED |
| Q01105 | Y146 | Sugiyama | SET | tEFEDIKsGyRIDFyFDENPyFENKVLSKEFHLNEsGDPss |
| Q01130 | Y44 | Sugiyama | SRSF2 SFRS2 | RtsPDtLRRVFEKYGRVGDVyIPRDRYTKESRGFAFVRFHD |
| Q01518 | T165 | Sugiyama | CAP1 CAP | AMAPKPGPYVKEMNDAAMFytNRVLKEYKDVDKKHVDWVKA |
| Q01518 | Y164 | Sugiyama | CAP1 CAP | VAMAPKPGPYVKEMNDAAMFytNRVLKEYKDVDKKHVDWVK |
| Q01814 | Y1152 | Sugiyama | ATP2B2 PMCA2 | RGLNRIQtQIRVVKAFRssLyEGLEKPEsRtsIHNFMAHPE |
| Q01844 | Y278 | Sugiyama | EWSR1 EWS | SSSYGQQSsFRQDHPssMGVyGQESGGFSGPGENRSMSGPD |
| Q02878 | Y115 | Sugiyama | RPL6 TXREB1 | PVGGDKNGGTRVVKLRKMPRyyPtEDVPRKLLSHGKKPFSQ |
| Q04446 | Y657 | Sugiyama | GBE1 | RVGTALPGKFKIVLDSDAAEyGGHQRLDHSTDFFSEAFEHN |
| Q04446 | Y73 | Sugiyama | GBE1 | sQILKNIGENEGGIDKFSRGyEsFGVHRCADGGLYCKEWAP |
| Q04637 | Y594 | Sugiyama | EIF4G1 EIF4F EIF4G EIF4GI | WDSKEDKIHNAENIQPGEQKyEyKsDQWKPLNLEEKKRYDR |
| Q04637 | Y596 | Sugiyama | EIF4G1 EIF4F EIF4G EIF4GI | SKEDKIHNAENIQPGEQKyEyKsDQWKPLNLEEKKRYDREF |
| Q04760 | Y136 | SIGNOR|PSP | GLO1 | HNGNsDPRGFGHIGIAVPDVySACKRFEELGVKFVKKPDDG |
| Q04837 | Y73 | Sugiyama | SSBP1 SSBP | PVTIFSLATNEMWRsGDsEVyQLGDVsQKTTWHRISVFRPG |
| Q04917 | Y154 | Sugiyama | YWHAH YWHA1 | LAEVASGEKKNsVVEAsEAAyKEAFEISKEQMQPTHPIRLG |
| Q04917 | Y49 | Sugiyama | YWHAH YWHA1 | AVtELNEPLsNEDRNLLsVAyKNVVGARRSsWRVIsSIEQK |
| Q05639 | Y254 | Sugiyama | EEF1A2 EEF1AL STN | TILPPTRPTDKPLRLPLQDVyKIGGIGtVPVGRVETGILRP |
| Q05639 | Y29 | Sugiyama | EEF1A2 EEF1AL STN | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| Q05655 | Y155 | iPTMNet|EPSD | PRKCD PKCD | DEAKFPtMNRRGAIKQAKIHyIKNHEFIATFFGQPTFCSVC |
| Q05655 | Y187 | iPTMNet|EPSD | PRKCD PKCD | GQPTFCSVCKDFVWGLNKQGyKCRQCNAAIHKKCIDKIIGR |
| Q05655 | Y52 | SIGNOR|iPTMNet|EPSD | PRKCD PKCD | MKEALSTERGKTLVQKKPTMyPEWKStFDAHIyEGRVIQIV |
| Q05655 | Y567 | SIGNOR|iPTMNet|EPSD | PRKCD PKCD | PFHGDDEDELFESIRVDTPHyPRWITKESKDILEKLFEREP |
| Q05655 | Y64 | iPTMNet|EPSD | PRKCD PKCD | LVQKKPTMyPEWKStFDAHIyEGRVIQIVLMRAAEEPVSEV |
| Q06187 | Y223 | EPSD|PSP | BTK AGMX1 ATK BPK | PPEPAAAPVSTSELKKVVALyDyMPMNANDLQLRKGDEYFI |
| Q06187 | Y551 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | BTK AGMX1 ATK BPK | DQGVVKVSDFGLsRyVLDDEytssVGsKFPVRWSPPEVLMY |
| Q06830 | Y116 | Sugiyama | PRDX1 PAGA PAGB TDPX2 | GLGPMNIPLVSDPKRtIAQDyGVLKADEGIsFRGLFIIDDK |
| Q06830 | Y34 | Sugiyama | PRDX1 PAGA PAGB TDPX2 | NFKAtAVMPDGQFKDIsLsDyKGKYVVFFFYPLDFTFVCPT |
| Q07866 | Y449 | Sugiyama | KLC1 KLC KNS2 | HAEEREECKGKQKDGTsFGEyGGWyKACKVDsPtVTTtLKN |
| Q07866 | Y453 | Sugiyama | KLC1 KLC KNS2 | REECKGKQKDGTsFGEyGGWyKACKVDsPtVTTtLKNLGAL |
| Q07955 | Y37 | Sugiyama | SRSF1 ASF SF2 SF2P33 SFRS1 OK/SW-cl.3 | RIyVGNLPPDIRtKDIEDVFyKYGAIRDIDLKNRRGGPPFA |
| Q08043 | Y229 | Sugiyama | ACTN3 | KLRKDDPIGNLNTAFEVAEKyLDIPKMLDAEDIVNtPKPDE |
| Q08378 | Y512 | Sugiyama | GOLGA3 | EAKNAsLAssNNDLQVAEEQyQRLMAKVEDMQRSMLSKDNT |
| Q08J23 | Y52 | Sugiyama | NSUN2 SAKI TRM4 | AGWEGGyPEIVKENKLFEHyyQELKIVPEGEWGQFMDALRE |
| Q12797 | Y90 | Sugiyama | ASPH BAH | VAVVWFDLVDYEEVLGKLGIyDADGDGDFDVDDAKVLLGLK |
| Q12805 | Y65 | Sugiyama | EFEMP1 FBLN3 FBNL | IDECDIVPDACKGGMKCVNHyGGyLCLPKTAQIIVNNEQPQ |
| Q12805 | Y68 | Sugiyama | EFEMP1 FBLN3 FBNL | CDIVPDACKGGMKCVNHyGGyLCLPKTAQIIVNNEQPQQET |
| Q12874 | Y85 | Sugiyama | SF3A3 SAP61 | DGLRKEELNAIsGPNEFAEFyNRLKQIKEFHRKHPNEICVP |
| Q12931 | Y498 | Sugiyama | TRAP1 HSP75 HSPC5 | GQLtsLsEyASRMRAGtRNIyyLCAPNRHLAEHsPyyEAMK |
| Q12931 | Y513 | Sugiyama | TRAP1 HSP75 HSPC5 | GtRNIyyLCAPNRHLAEHsPyyEAMKKKDTEVLFCFEQFDE |
| Q12931 | Y514 | Sugiyama | TRAP1 HSP75 HSPC5 | tRNIyyLCAPNRHLAEHsPyyEAMKKKDTEVLFCFEQFDEL |
| Q12972 | Y264 | GPS6|SIGNOR|ELM|iPTMNet|EPSD | PPP1R8 ARD1 NIPP1 | LGLEEsGSRRMQNFAFSGGLyGGLPPTHSEAGSQPHGIHGT |
| Q12972 | Y335 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | PPP1R8 ARD1 NIPP1 | PAPNPAVYNPEAVNEPKKKKyAKEAWPGKKPTPSLLI____ |
| Q12996 | Y708 | Sugiyama | CSTF3 | NEDsDEDEEKGAVVPPVHDIyRARQQKRIR___________ |
| Q13069 | Y10 | Sugiyama | GAGE5 | ___________MSWRGRsTyyWPRPRRYVQPPEVIGPMRPE |
| Q13069 | Y9 | Sugiyama | GAGE5 | ____________MSWRGRsTyyWPRPRRYVQPPEVIGPMRP |
| Q13070 | Y10 | Sugiyama | GAGE6 | ___________MSWRGRsTyyWPRPRRYVQPPEVIGPMRPE |
| Q13070 | Y9 | Sugiyama | GAGE6 | ____________MSWRGRsTyyWPRPRRYVQPPEVIGPMRP |
| Q13228 | Y28 | Sugiyama | SELENBP1 SBP | CGPGySTPLEAMKGPREEIVyLPCIyRNtGtEAPDyLATVD |
| Q13228 | Y33 | Sugiyama | SELENBP1 SBP | STPLEAMKGPREEIVyLPCIyRNtGtEAPDyLATVDVDPKs |
| Q13242 | Y17 | Sugiyama | SRSF9 SFRS9 SRP30C | ____MsGWADERGGEGDGRIyVGNLPTDVREKDLEDLFyKY |
| Q13242 | Y70 | Sugiyama | SRSF9 SFRS9 SRP30C | GLVPFAFVRFEDPRDAEDAIyGRNGyDYGQCRLRVEFPRTY |
| Q13263 | Y242 | Sugiyama | TRIM28 KAP1 RNF96 TIF1B | ESCDTLTCRDCQLNAHKDHQyQFLEDAVRNQRKLLAsLVKR |
| Q13263 | Y449 | EPSD|PSP | TRIM28 KAP1 RNF96 TIF1B | PGPLSKQGsGssQPMEVQEGyGFGsGDDPyssAEPHVsGVK |
| Q13263 | Y458 | EPSD|PSP | TRIM28 KAP1 RNF96 TIF1B | GssQPMEVQEGyGFGsGDDPyssAEPHVsGVKRsRsGEGEV |
| Q13263 | Y517 | EPSD|PSP | TRIM28 KAP1 RNF96 TIF1B | LtADsQPPVFKVFPGsttEDyNLIVIERGAAAAATGQPGtA |
| Q13283 | Y125 | Sugiyama | G3BP1 G3BP | LRRFMQtFVLAPEGsVANKFyVHNDIFRyQDEVFGGFVtEP |
| Q13283 | Y19 | Sugiyama | G3BP1 G3BP | __MVMEKPsPLLVGREFVRQyytLLNQAPDMLHRFYGKNss |
| Q13283 | Y20 | Sugiyama | G3BP1 G3BP | _MVMEKPsPLLVGREFVRQyytLLNQAPDMLHRFYGKNssy |
| Q13283 | Y363 | Sugiyama | G3BP1 G3BP | FIGNLPHEVDKSELKDFFQsyGNVVELRINsGGKLPNFGFV |
| Q13283 | Y56 | Sugiyama | G3BP1 G3BP | KNssyVHGGLDsNGKPADAVyGQKEIHRKVMsQNFtNCHTK |
| Q13291 | Y327 | GPS6|SIGNOR|ELM|iPTMNet|EPSD|PSP | SLAMF1 SLAM | yVAATEPVPESVQETNSITVyASVTLPES____________ |
| Q13303 | Y270 | Sugiyama | KCNAB2 KCNA2B KCNK2 | IVSGKYDSGIPPYSRAsLKGyQWLKDKILSEEGRRQQAKLK |
| Q13310 | Y194 | Sugiyama | PABPC4 APP1 PABP4 | KSRKEREAELGAKAKEFtNVyIKNFGEEVDDEsLKELFsQF |
| Q13404 | Y145 | Sugiyama | UBE2V1 CROC1 UBE2V UEV1 P/OKcl.19 | RRLMMSKENMKLPQPPEGQCysN__________________ |
| Q13435 | Y591 | Sugiyama | SF3B2 SAP145 | LHDAFFKWQTKPKLTIHGDLyyEGKEFETRLKEKKPGDLSD |
| Q13435 | Y592 | Sugiyama | SF3B2 SAP145 | HDAFFKWQTKPKLTIHGDLyyEGKEFETRLKEKKPGDLSDE |
| Q13442 | Y70 | Sugiyama | PDAP1 HASPP28 | DPKKEKKsLDsDEsEDEEDDyQQKRKGVEGLIDIENPNRVA |
| Q13509 | T107 | Sugiyama | TUBB3 TUBB4 | PDNFIFGQSGAGNNWAKGHytEGAELVDsVLDVVRKECENC |
| Q13509 | Y106 | Sugiyama | TUBB3 TUBB4 | RPDNFIFGQSGAGNNWAKGHytEGAELVDsVLDVVRKECEN |
| Q13510 | Y305 | Sugiyama | ASAH1 ASAH HSD-33 HSD33 | GNQSGEGCVITRDRKESLDVyELDAKQGRWYVVQTNYDRWK |
| Q13546 | Y387 | Sugiyama | RIPK1 RIP RIP1 | QEENEPSLQSKLQDEANyHLyGsRMDRQTKQQPRQNVAYNR |
| Q13561 | Y313 | Sugiyama | DCTN2 DCTN50 | IAKHKASVEDADTQSKVHQLyEtIQRWsPIASTLPELVQRL |
| Q13561 | Y6 | Sugiyama | DCTN2 DCTN50 | _______________MADPKyADLPGIARNEPDVYETSDLP |
| Q13561 | Y86 | Sugiyama | DCTN2 DCTN50 | GLDFsDRIGKTKRtGyEsGEyEMLGEGLGVKETPQQKYQRL |
| Q13568 | Y313 | SIGNOR|EPSD|PSP | IRF5 | sLEQVRFPsPEDIPSDKQRFyTNQLLDVLDRGLILQLQGQD |
| Q13568 | Y335 | SIGNOR|EPSD|PSP | IRF5 | NQLLDVLDRGLILQLQGQDLyAIRLCQCKVFWSGPCASAHD |
| Q13573 | Y430 | Sugiyama | SNW1 SKIIP SKIP | RLFNQSKGMDSGFAGGEDEIyNVyDQAWRGGKDMAQsIyRP |
| Q13573 | Y433 | Sugiyama | SNW1 SKIIP SKIP | NQSKGMDSGFAGGEDEIyNVyDQAWRGGKDMAQsIyRPSKN |
| Q13596 | Y162 | Sugiyama | SNX1 | QFDLTVGITDPEKIGDGMNAyVAyKVTTQTsLPLFRSKQFA |
| Q13601 | Y287 | Sugiyama | KRR1 HRB2 | tPFPPPQPESQIDKELAsGEyFLKANQKKRQKMEAIKAKQA |
| Q13642 | Y149 | Sugiyama | FHL1 SLIM1 | CSNCKQVIGtGSFFPKGEDFyCVtCHETKFAKHCVKCNKAI |
| Q13642 | Y9 | Sugiyama | FHL1 SLIM1 | ____________MAEKFDCHyCRDPLQGKKYVQKDGHHCCL |
| Q13765 | Y120 | Sugiyama | NACA HSD48 | KNILFVITKPDVYKSPAsDtyIVFGEAKIEDLsQQAQLAAA |
| Q13885 | T107 | Sugiyama | TUBB2A TUBB2 | PDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKESESC |
| Q13885 | Y106 | Sugiyama | TUBB2A TUBB2 | RPDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKESES |
| Q14118 | Y524 | Sugiyama | DAG1 | DRVDAWVGTYFEVKIPSDtFyDHEDTTTDKLKLTLKLREQQ |
| Q14152 | Y697 | Sugiyama | EIF3A EIF3S10 KIAA0139 | LEKEKKELQERLKNQEKKIDyFERAKRLEEIPLIKSAYEEQ |
| Q14157 | Y858 | Sugiyama | UBAP2L KIAA0144 NICE4 | PFPtPttPLtGRDGsLAsNPysGDLtKFGRGDASSPAPATT |
| Q14240 | Y71 | Sugiyama | EIF4A2 DDX2B EIF4F | yGFEKPsAIQQRAIIPCIKGyDVIAQAQsGtGKTATFAISI |
| Q14247 | Y215 | Sugiyama | CTTN EMS1 | FGGKyGIDKDKVDKsAVGFEyQGKtEKHESQKDyVKGFGGK |
| Q14247 | Y334 | Sugiyama | CTTN EMS1 | KDRMDKNAstFEDVtQVssAyQKTVPVEAVtsKtsNIRANF |
| Q14247 | Y446 | Sugiyama | CTTN EMS1 | sFKAELsyRGPVsGtEPEPVysMEAADyREASSQQGLAYAT |
| Q14257 | Y311 | Sugiyama | RCN2 ERC55 | NPDLFLtsEAtDyGRQLHDDyFyHDEL______________ |
| Q14257 | Y313 | Sugiyama | RCN2 ERC55 | DLFLtsEAtDyGRQLHDDyFyHDEL________________ |
| Q14289 | Y579 | GPS6|EPSD | PTK2B FAK2 PYK2 RAFTK | SPECVKLGDFGLsRYIEDEDyyKASVTRLPIKWMSPESINF |
| Q14289 | Y580 | GPS6 | PTK2B FAK2 PYK2 RAFTK | PECVKLGDFGLsRYIEDEDyyKASVTRLPIKWMSPESINFR |
| Q14566 | Y810 | Sugiyama | MCM6 | LTQAGLKGstEGsEsYEEDPyLVVNPNyLLED_________ |
| Q14568 | Y283 | Sugiyama | HSP90AA2P HSP90AA2 HSPC2 HSPCAL3 | sDEEEEKKDGDKKKKKTKEKyIDQEELNKTKPIWTRNPDDI |
| Q14671 | Y83 | Sugiyama | PUM1 KIAA0099 PUMH1 | SPVPGSIGVAGRsQDDAMVDyFFQRQHGEQLGGGGsGGGGy |
| Q14697 | Y489 | Sugiyama | GANAB G2AN KIAA0088 | PHIKVDSGyRVHEELRNLGLyVKtRDGSDyEGWCWPGSAGY |
| Q14697 | Y563 | Sugiyama | GANAB G2AN KIAA0088 | MNEPSVFNGPEVTMLKDAQHyGGWEHRDVHNIYGLYVHMAT |
| Q14790 | Y380 | SIGNOR|EPSD|PSP | CASP8 MCH5 | CQGDNYQKGIPVETDSEEQPyLEMDLSsPQTRYIPDEADFL |
| Q14790 | Y448 | SIGNOR|EPSD|PSP | CASP8 MCH5 | SLRERCPRGDDILTILTEVNyEVSNKDDKKNMGKQMPQPTF |
| Q14847 | Y171 | PSP | LASP1 MLN50 | syRRPLEQQQPHHIPtsAPVyQQPQQQPVAQsYGGyKEPAA |
| Q14974 | Y529 | Sugiyama | KPNB1 NTF97 | KLLETTDRPDGHQNNLRSSAyEsLMEIVKNSAKDCYPAVQK |
| Q15024 | Y187 | Sugiyama | EXOSC7 KIAA0116 RRP42 | RVRVLEDEEGsKDIELSDDPyDCIRLSVENVPCIVTLCKIG |
| Q15056 | Y101 | Sugiyama | EIF4H KIAA0038 WBSCR1 WSCR1 | FKGFCyVEFDEVDsLKEALtyDGALLGDRsLRVDIAEGRKQ |
| Q15149 | Y3362 | Sugiyama | PLEC PLEC1 | TGLsLLPLSEKAARARQEELySELQAREtFEKTPVEVPVGG |
| Q15293 | Y148 | Sugiyama | RCN1 RCN | DRDKDDKISWEEyKQAtyGyyLGNPAEFHDssDHHtFKKML |
| Q15293 | Y278 | Sugiyama | RCN1 RCN | LNKDGKLDKDEIRHWILPQDyDHAQAEARHLVyESDKNKDE |
| Q15369 | Y18 | Sugiyama | ELOC TCEB1 | ___MDGEEKtyGGCEGPDAMyVKLISSDGHEFIVKREHALt |
| Q15369 | Y8 | Sugiyama | ELOC TCEB1 | _____________MDGEEKtyGGCEGPDAMyVKLISSDGHE |
| Q15417 | Y261 | Sugiyama | CNN3 | STISLQMGTNKVAsQKGMsVyGLGRQVYDPKYCAAPTEPVI |
| Q15427 | Y16 | Sugiyama | SF3B4 SAP49 | _____MAAGPISERNQDAtVyVGGLDEKVSEPLLWELFLQA |
| Q15459 | S451 | Sugiyama | SF3A1 SAP114 | IGLLDPRWLEQRDRSIREKQsDDEVyAPGLDIESsLKQLAE |
| Q15459 | Y456 | Sugiyama | SF3A1 SAP114 | PRWLEQRDRSIREKQsDDEVyAPGLDIESsLKQLAERRtDI |
| Q15527 | Y123 | Sugiyama | SURF2 | GRRYQRALCKYEECQKQGVEyVPACLVHRRRRREDQMDGDG |
| Q15631 | Y210 | Sugiyama | TSN | sLRKRYDGLKYDVKKVEEVVyDLSIRGFNKETAAACVEK__ |
| Q15637 | Y87 | Sugiyama | SF1 ZFM1 ZNF162 | tGDLGIPPNPEDRsPsPEPIyNsEGKRLNTREFRTRKKLEE |
| Q15642 | Y190 | Sugiyama | TRIP10 CIP4 STOT STP | EKAKQQAHLRSHMAEESKNEyAAQLQRFNRDQAHFYFSQMP |
| Q15785 | Y25 | Sugiyama | TOMM34 URCC3 | FPDsVEELRAAGNESFRNGQyAEASALyGRALRVLQAQGss |
| Q15785 | Y32 | Sugiyama | TOMM34 URCC3 | LRAAGNESFRNGQyAEASALyGRALRVLQAQGssDPEEEsV |
| Q15819 | Y143 | Sugiyama | UBE2V2 MMS2 UEV2 | RRLMMSKENMKLPQPPEGQtyNN__________________ |
| Q16719 | Y441 | Sugiyama | KYNU | RGVVCDKRNPNGIRVAPVPLyNsFHDVyKFTNLLtsILDsA |
| Q16719 | Y448 | Sugiyama | KYNU | RNPNGIRVAPVPLyNsFHDVyKFTNLLtsILDsAETKN___ |
| Q16719 | Y47 | Sugiyama | KYNU | ERVALHLDEEDKLRHFRECFyIPKIQDLPPVDLSLVNKDEN |
| Q16719 | Y86 | Sugiyama | KYNU | ENAIYFLGNSLGLQPKMVKtyLEEELDKWAKIAAYGHEVGK |
| Q16763 | Y144 | Sugiyama | UBE2S E2EPF OK/SW-cl.73 | NPESALNEEAGRLLLENyEEyAARARLLtEIHGGAGGPSGR |
| Q16778 | Y41 | Sugiyama | H2BC21 H2BFQ HIST2H2BE | KAQKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGIssKAMG |
| Q16778 | Y43 | Sugiyama | H2BC21 H2BFQ HIST2H2BE | QKKDGKKRKRSRKEsysIyVyKVLKQVHPDTGIssKAMGIM |
| Q16851 | Y89 | Sugiyama | UGP2 UGP1 | KGPSVDWGKIQRPPEDSIQPyEKIKARGLPDNISsVLNKLV |
| Q2NKX8 | Y1200 | Sugiyama | ERCC6L PICH | LsGEQLVGsPQDKAAEATNDyEtLVKRGKELKECGKIQEAL |
| Q4VXU2 | Y297 | Sugiyama | PABPC1L C20orf119 | KRRFEQMKQDRLRRyQGVNLyVKNLDDSIDDDKLRKEFSPY |
| Q53H82 | Y99 | Sugiyama | LACTB2 CGI-83 | HRDHSGGIGDICKSINNDtTyCIKKLPRNPQREEIIGNGEQ |
| Q562R1 | S240 | Sugiyama | ACTBL2 | VALDFEQEMVRAAAssSPERsyELPDGQVItIGNERFRCPE |
| Q562R1 | Y241 | Sugiyama | ACTBL2 | ALDFEQEMVRAAAssSPERsyELPDGQVItIGNERFRCPEA |
| Q58FF3 | Y58 | Sugiyama | HSP90B2P GRP94B GRP94P1 TRAP1 | VTFKSILFVPTFVPRGLFDEyGsKKSDYIKLYVRCVFITDD |
| Q58FF6 | Y167 | Sugiyama | HSP90AB4P | GEPIDRDTKVILHLKEDQtEyLEERWVKEVVKKHPQFIGCL |
| Q58FF6 | Y32 | Sugiyama | HSP90AB4P | KEIFLQELISNASDALDKIRyEsLtDPsKLDGGKELKIDII |
| Q58FF7 | Y171 | Sugiyama | HSP90AB3P HSP90BC | GEPIGRGTKVILHLKEDQtEyLEERRVKEVVKKHsQFIGyP |
| Q58FF7 | Y492 | Sugiyama | HSP90AB3P HSP90BC | TANMEQIMKAQALRDNstMGyMMAKKHLEINPDHPIMETLR |
| Q58FF7 | Y56 | Sugiyama | HSP90AB3P HSP90BC | EEIFLQELISNASDALDKIRyEsLtDPsKLDsGKELKIDII |
| Q58FF8 | Y198 | Sugiyama | HSP90AB2P HSP90BB | DEEDDsGKDKKKKTKKIKEKyIDQEELNKTKPIWTRNTEDI |
| Q58FF8 | Y260 | Sugiyama | HSP90AB2P HSP90BB | VRYFSVEEYVSRMKEIQKsIyyItGEsKEQVANSAFVEQVW |
| Q58FF8 | Y261 | Sugiyama | HSP90AB2P HSP90BB | RYFSVEEYVSRMKEIQKsIyyItGEsKEQVANSAFVEQVWK |
| Q58FF8 | Y56 | Sugiyama | HSP90AB2P HSP90BB | KEIFLWELISNASDALDKIRyEsLtDPsKLDsGKELKIDII |
| Q58FG0 | Y177 | Sugiyama | HSP90AA5P HSP90AE | GQLEELKDSRRVMKANQKHIyyItGETKDQVANSAFVECLQ |
| Q58FG0 | Y178 | Sugiyama | HSP90AA5P HSP90AE | QLEELKDSRRVMKANQKHIyyItGETKDQVANSAFVECLQK |
| Q5F1R6 | Y5 | Sugiyama | DNAJC21 DNAJA5 | ________________MKCHyEALGVRRDASEEELKKAYRK |
| Q5JTH9 | Y1251 | Sugiyama | RRP12 KIAA0690 | AEYKAKKAKGDVKKKGRPDPyAyIPLNRSKLNRRKKMKLQG |
| Q5JTH9 | Y1253 | Sugiyama | RRP12 KIAA0690 | YKAKKAKGDVKKKGRPDPyAyIPLNRSKLNRRKKMKLQGQF |
| Q5QNW6 | Y41 | Sugiyama | H2BC18 HIST2H2BF | KVQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q5QNW6 | Y43 | Sugiyama | H2BC18 HIST2H2BF | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q5SW79 | Y364 | Sugiyama | CEP170 FAM68A KAB KIAA0470 | QMLWERTEEDsKsIKsDVPVyLKRLKGNKHDDGtQsDsENA |
| Q5VTE0 | T88 | Sugiyama | EEF1A1P5 EEF1AL3 | ERGITIDISLWKFEtsKyyVtIIDAPGHRDFIKNMITGTSQ |
| Q5VTE0 | Y254 | Sugiyama | EEF1A1P5 EEF1AL3 | CILPPtRPTDKPLRLPLQDVyKIGGIGtVPVGRVEtGVLKP |
| Q5VTE0 | Y29 | Sugiyama | EEF1A1P5 EEF1AL3 | NIVVIGHVDsGKstttGHLIyKCGGIDKRTIEKFEKEAAEM |
| Q5VTE0 | Y85 | Sugiyama | EEF1A1P5 EEF1AL3 | AERERGITIDISLWKFEtsKyyVtIIDAPGHRDFIKNMITG |
| Q5VTE0 | Y86 | Sugiyama | EEF1A1P5 EEF1AL3 | ERERGITIDISLWKFEtsKyyVtIIDAPGHRDFIKNMITGT |
| Q5VV41 | Y216 | Sugiyama | ARHGEF16 EPHEXIN4 NBR | KKTLGRKRGHKGsFKDDPQLyQEIQERGLNtsQEsDDDILD |
| Q6DN03 | Y41 | Sugiyama | H2BC20P HIST2H2BC | KAQKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMG |
| Q6DN03 | Y43 | Sugiyama | H2BC20P HIST2H2BC | QKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMGIM |
| Q6DRA6 | Y41 | Sugiyama | H2BC19P HIST2H2BD | KAQKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMG |
| Q6DRA6 | Y43 | Sugiyama | H2BC19P HIST2H2BD | QKKDGKKRKRSRKEsysIyVyKVLKRVHPDTGIWCKAMGIM |
| Q6L8Q7 | Y235 | Sugiyama | PDE12 | sLsPssPsssWtEtDVEERVytPSNADIGLRLKLHCTPGDG |
| Q6PEY2 | T225 | Sugiyama | TUBA3E | DNEAIYDICRRNLDIERPtytNLNRLIGQIVSSITASLRFD |
| Q6PKG0 | Y633 | Sugiyama | LARP1 KIAA0731 LARP | MEQMDGRKNtFtAWsDEEsDyEIDDRDVNKILIVtQtPHyM |
| Q6S8J3 | S939 | Sugiyama | POTEE A26C1A POTE2 | VALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPE |
| Q6S8J3 | Y1062 | Sugiyama | POTEE A26C1A POTE2 | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| Q6S8J3 | Y791 | Sugiyama | POTEE A26C1A POTE2 | MEHGIITNWDDMEKIWHHtFyNELRVAPEEHPILLTEAPLN |
| Q6S8J3 | Y940 | Sugiyama | POTEE A26C1A POTE2 | ALDFEQEMAtAAssssLEKsyELPDGQVItIGNERFRCPEA |
| Q6UVK1 | Y1511 | Sugiyama | CSPG4 MCSP | PIPAEALRSTDGDSGSEDLVyTIEQPSNGRVVLRGAPGTEV |
| Q71U36 | T225 | Sugiyama | TUBA1A TUBA3 | DNEAIYDICRRNLDIERPtytNLNRLIGQIVSSITASLRFD |
| Q71U36 | Y103 | Sugiyama | TUBA1A TUBA3 | yRQLFHPEQLItGKEDAANNyARGHYTIGKEIIDLVLDRIR |
| Q71U36 | Y432 | Sugiyama | TUBA1A TUBA3 | GMEEGEFSEAREDMAALEKDyEEVGVDsVEGEGEEEGEEy_ |
| Q71U36 | Y451 | Sugiyama | TUBA1A TUBA3 | DyEEVGVDsVEGEGEEEGEEy____________________ |
| Q7KZF4 | S474 | Sugiyama | SND1 TDRD11 | LVSKGLATVIRYRQDDDQRssHyDELLAAEARAIKNGKGLH |
| Q7RTV0 | Y100 | Sugiyama | PHF5A | KDRDGCPKIVNLGSsKTDLFyERKKYGFKKR__________ |
| Q7RTV0 | Y51 | Sugiyama | PHF5A | VICDSyVRPCTLVRICDECNyGsyQGRCVICGGPGVSDAyy |
| Q7Z6I8 | Y35 | Sugiyama | C5orf24 | PGKPSCLNEDAMRAADQFDIySsQQsKYSHTVNHKPMVCQR |
| Q86SX6 | Y88 | Sugiyama | GLRX5 C14orf87 | GFSNAVVQILRLHGVRDyAAyNVLDDPELRQGIKDYSNWPT |
| Q86V81 | Y250 | Sugiyama | ALYREF ALY BEF THOC4 | AGRNSKQQLsAEELDAQLDAyNARMDts_____________ |
| Q86X76 | Y319 | Sugiyama | NIT1 | NyLRQLRRHLPVFQHRRPDLyGNLGHPLS____________ |
| Q8IV48 | Y66 | Sugiyama | ERI1 3'EXO THEX1 | QETKGSKFITssAsDFsDPVyKEIAITNGCINRMSKEELRA |
| Q8IV50 | Y213 | Sugiyama | LYSMD2 | AAKKLKEESRDEEsPyAtSLyHs__________________ |
| Q8N0Y7 | S134 | Sugiyama | PGAM4 PGAM3 | IWRRsyDVPPPPMEPDHPFysNIsKDRRYADLTEDQLPSYE |
| Q8N0Y7 | S137 | Sugiyama | PGAM4 PGAM3 | RsyDVPPPPMEPDHPFysNIsKDRRYADLTEDQLPSYESPK |
| Q8N0Y7 | Y119 | Sugiyama | PGAM4 PGAM3 | NKAETAAKHGEAQVKIWRRsyDVPPPPMEPDHPFysNIsKD |
| Q8N0Y7 | Y92 | Sugiyama | PGAM4 PGAM3 | DAIDQMWLPVVRTWRLNERHyGGLtGLNKAETAAKHGEAQV |
| Q8N1G4 | Y257 | Sugiyama | LRRC47 KIAA1185 | LRDKRLEKMVSGCQTRSILEyLRVGGRGGGKGKGRAEGSEK |
| Q8N257 | Y41 | Sugiyama | H2BC26 H2BU1 HIST3H2BB | KAQKKDGKKRKRGRKEsysIyVyKVLKQVHPDTGIssKAMG |
| Q8N257 | Y43 | Sugiyama | H2BC26 H2BU1 HIST3H2BB | QKKDGKKRKRGRKEsysIyVyKVLKQVHPDTGIssKAMGIM |
| Q8N6F7 | Y106 | SIGNOR|PSP | GCSAM GAL GCET2 | yTLINHRVLCTRPsGNsAEEyyENVPCKAERPREsLGGtEt |
| Q8N6F7 | Y107 | SIGNOR|EPSD|PSP | GCSAM GAL GCET2 | TLINHRVLCTRPsGNsAEEyyENVPCKAERPREsLGGtEtE |
| Q8N6F7 | Y128 | SIGNOR|EPSD|PSP | GCSAM GAL GCET2 | ENVPCKAERPREsLGGtEtEysLLHMPSTDPRHARsPEDEy |
| Q8N6F7 | Y80 | SIGNOR|PSP | GCSAM GAL GCET2 | SQNENERMSstPIQDNVDQtySEELCyTLINHRVLCTRPsG |
| Q8N6F7 | Y86 | SIGNOR|PSP | GCSAM GAL GCET2 | RMSstPIQDNVDQtySEELCyTLINHRVLCTRPsGNsAEEy |
| Q8N6H7 | Y278 | Sugiyama | ARFGAP2 ZNF289 Nbla10535 | QAADAKKQAEESMVASMRLAyQELQIDRKKEEKKLQNLEGK |
| Q8N6T3 | Y175 | Sugiyama | ARFGAP1 ARF1GAP | sVtAssDKAFEDWLNDDLGsyQGAQGNRyVGFGNtPPPQKK |
| Q8N7H5 | Y169 | Sugiyama | PAF1 PD2 | EKPEVKIGVSVKQQFTEEEIyKDRDSQITAIEKTFEDAQKS |
| Q8NBS9 | Y251 | Sugiyama | TXNDC5 TLP46 UNQ364/PRO700 | ALGLEHSETVKIGKVDCtQHyELCsGNQVRGyPtLLWFRDG |
| Q8NE71 | Y250 | Sugiyama | ABCF1 ABC50 | EEGEGEEEEEEGGESKADDPyAHLSKKEKKKLKKQMEYERQ |
| Q8NFI4 | Y185 | Sugiyama | ST13P5 FAM10A5 | NAAIQDCDRAIEINPDsAQPyKWRGKAHRLLGHWEEAAHDL |
| Q8NI22 | Y138 | Sugiyama | MCFD2 SDNSF | INIIDGVLRDDDKNNDGyIDyAEFAKSLQ____________ |
| Q8TD19 | Y52 | Sugiyama | NEK9 KIAA1995 NEK8 NERCC | PSASQGPRAGGGAAEQEELHyIPIRVLGRGAFGEAtLyRRT |
| Q8WWM7 | S276 | Sugiyama | ATXN2L A2D A2LG A2LP A2RP | MFKFNEENyGVKTtyDssLssytVPLEKDNsEEFRQRELRA |
| Q8WWM7 | Y270 | Sugiyama | ATXN2L A2D A2LG A2LP A2RP | GWDPNEMFKFNEENyGVKTtyDssLssytVPLEKDNsEEFR |
| Q92522 | Y48 | Sugiyama | H1-10 H1FX | AALsPsKKRKNSKKKNQPGKySQLVVEtIRRLGERNGSSLA |
| Q92598 | Y641 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | MIMQDKLEKERNDAKNAVEEyVyEFRDKLCGPYEKFICEQD |
| Q92598 | Y643 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | MQDKLEKERNDAKNAVEEyVyEFRDKLCGPYEKFICEQDHQ |
| Q92598 | Y677 | Sugiyama | HSPH1 HSP105 HSP110 KIAA0201 | ICEQDHQNFLRLLTETEDWLyEEGEDQAKQAyVDKLEELMK |
| Q92796 | S615 | Sugiyama | DLG3 KIAA1232 | GLSDDYYGAKNLKGQEDAILsYEPVTRQEIHYARPVIILGP |
| Q92882 | Y207 | Sugiyama | OSTF1 | sLLKKKQGTDAVRtLsNAEDyLDDEDsD_____________ |
| Q92918 | Y381 | SIGNOR|EPSD | MAP4K1 HPK1 | PRDLRSSSPRKQLsEssDDDyDDVDIPTPAEDTPPPLPPKP |
| Q93052 | T316 | Sugiyama | LPP | yyEGyyAAGPGyGGRNDsDPtyGQQGHPNtWKREPGytPPG |
| Q93052 | Y297 | Sugiyama | LPP | PPPGLQPEPGYGYAPNQGRyyEGyyAAGPGyGGRNDsDPty |
| Q93052 | Y301 | Sugiyama | LPP | LQPEPGYGYAPNQGRyyEGyyAAGPGyGGRNDsDPtyGQQG |
| Q93052 | Y317 | Sugiyama | LPP | yEGyyAAGPGyGGRNDsDPtyGQQGHPNtWKREPGytPPGA |
| Q93079 | Y41 | Sugiyama | H2BC9 H2BFJ HIST1H2BH | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q93079 | Y43 | Sugiyama | H2BC9 H2BFJ HIST1H2BH | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q969T4 | Y91 | Sugiyama | UBE2E3 UBCE4 UBCH9 | AEITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| Q96A49 | Y327 | Sugiyama | SYAP1 PRO3113 | AVLEEDsADWEKELQQELQEyEVVtESEKRDENWDKEIEKM |
| Q96AE4 | Y58 | Sugiyama | FUBP1 | ARQIAAKIGGDAGtsLNsNDyGyGGQKRPLEDGDQPDAKKV |
| Q96AE4 | Y60 | Sugiyama | FUBP1 | QIAAKIGGDAGtsLNsNDyGyGGQKRPLEDGDQPDAKKVAP |
| Q96AY3 | Y201 | Sugiyama | FKBP10 FKBP65 PSEC0056 | YNGTLLDGTSFDTSYSKGGtyDtyVGsGWLIKGMDQGLLGM |
| Q96AY3 | Y204 | Sugiyama | FKBP10 FKBP65 PSEC0056 | TLLDGTSFDTSYSKGGtyDtyVGsGWLIKGMDQGLLGMCPG |
| Q96BY7 | Y2012 | Sugiyama | ATG2B C14orf103 | GVAKAYSVVKEGITDTAQTIyETAAREHESRGVTGAVGEVL |
| Q96C19 | T84 | Sugiyama | EFHD2 SWS1 | DLNQGIGEPQsPsRRVFNPytEFKEFSRKQIKDMEKMFKQy |
| Q96C19 | Y83 | Sugiyama | EFHD2 SWS1 | ADLNQGIGEPQsPsRRVFNPytEFKEFSRKQIKDMEKMFKQ |
| Q96CT7 | Y38 | Sugiyama | CCDC124 | RRAEAKAAADAKKQKELEDAyWKDDDKHVMRKEQRKEEKEK |
| Q96CW6 | Y300 | Sugiyama | SLC7A6OS | GSSRQRMWSKYPLDVQKEFGyDsPHDLDsD___________ |
| Q96DG6 | Y165 | Sugiyama | CMBL | YSEFRAGVSVYGIVKDSEDIyNLKNPTLFIFAENDVVIPLK |
| Q96F86 | Y225 | Sugiyama | EDC3 LSM16 YJDC YJEFN2 PP844 | DFEGNLALFDKAAVFEEIDtyERRSGTRsRGIPNERPTRYR |
| Q96FW1 | Y26 | Sugiyama | OTUB1 OTB1 OTU1 HSPC263 | PQQQKQEPLGsDsEGVNCLAyDEAIMAQQDRIQQEIAVQNP |
| Q96GX9 | Y57 | Sugiyama | APIP CGI-29 | HLGWVTGTGGGISLKHGDEIyIAPsGVQKERIQPEDMFVCD |
| Q96LR5 | Y85 | Sugiyama | UBE2E2 UBCH8 | AEITLDPPPNCSAGPKGDNIyEWRSTILGPPGSVYEGGVFF |
| Q96P70 | Y889 | Sugiyama | IPO9 IMP9 KIAA1192 RANBP9 HSPC273 | HGINADDKRLQDIRVKGEEIysMDEGIRTRSKSAKNPERWT |
| Q96QK1 | Y507 | Sugiyama | VPS35 MEM3 TCCCTA00141 | EQSLVGRFIHLLRsEDPDQQyLILNTARKHFGAGGNQRIRF |
| Q96QK1 | Y791 | Sugiyama | VPS35 MEM3 TCCCTA00141 | HNtLEHLRLRREsPEsEGPIyEGLIL_______________ |
| Q96ST3 | Y13 | Sugiyama | SIN3A | ________MKRRLDDQEsPVyAAQQRRIPGstEAFPHQHRV |
| Q96TC7 | Y176 | PSP | RMDN3 FAM82A2 FAM82C PTPIP51 hucep-10 UNQ3122/PRO10274 | SVYFTASSGATFTDAESEGGyTTANAESDNERDsDKEsEDG |
| Q99426 | Y107 | Sugiyama | TBCB CG22 CKAP1 | VIDHsGARLGEyEDVSRVEKytIsQEAyDQRQDtVRSFLKR |
| Q99426 | Y114 | Sugiyama | TBCB CG22 CKAP1 | RLGEyEDVSRVEKytIsQEAyDQRQDtVRSFLKRsKLGRyN |
| Q99459 | Y511 | Sugiyama | CDC5L KIAA0432 PCDC5RP | EIVLPENAEKELEEREIDDtyIEDAADVDARKQAIRDAERV |
| Q99459 | Y788 | Sugiyama | CDC5L KIAA0432 PCDC5RP | ECLKEDVQRQQEREKELQHRyADLLLEKETLKSKF______ |
| Q99460 | Y494 | Sugiyama | PSMD1 | RHGGSLGLGLAAMGTARQDVyDLLKTNLYQDDAVTGEAAGL |
| Q99497 | T140 | Sugiyama | PARK7 | GSKVTtHPLAKDKMMNGGHytysENRVEKDGLILtSRGPGT |
| Q99497 | Y141 | Sugiyama | PARK7 | SKVTtHPLAKDKMMNGGHytysENRVEKDGLILtSRGPGTS |
| Q99497 | Y67 | Sugiyama | PARK7 | sRDVVICPDAsLEDAKKEGPyDVVVLPGGNLGAQNLSESAA |
| Q99536 | Y240 | Sugiyama | VAT1 | TASASKHEALKENGVTHPIDyHttDyVDEIKKISPKGVDIV |
| Q99536 | Y245 | Sugiyama | VAT1 | KHEALKENGVTHPIDyHttDyVDEIKKISPKGVDIVMDPLG |
| Q99543 | Y274 | Sugiyama | DNAJC2 MPHOSPH11 MPP11 ZRF1 | TRAQRKKEEMNRIRtLVDNAysCDPRIKKFKEEEKAKKEAE |
| Q99613 | Y881 | Sugiyama | EIF3C EIF3S8 | EKLGsLVENNERVFDHKQGtyGGyFRDQKDGYRKNEGYMRR |
| Q99614 | Y280 | Sugiyama | TTC1 TPR1 | RPFGLstENFQIKQDsstGsysINFVQNPNNNR________ |
| Q99614 | Y96 | Sugiyama | TTC1 TPR1 | ADKVENKsNEDVNssELDEEyLIELEKNMSDEEKQKRREES |
| Q99733 | Y95 | Sugiyama | NAP1L4 NAP2 | VRCAHIEAKFyEEVHDLERKyAALyQPLFDKRREFItGDVE |
| Q99733 | Y99 | Sugiyama | NAP1L4 NAP2 | HIEAKFyEEVHDLERKyAALyQPLFDKRREFItGDVEPtDA |
| Q99798 | Y71 | Sugiyama | ACO2 | NINIVRKRLNRPLTLSEKIVyGHLDDPAsQEIERGKSYLRL |
| Q99848 | Y265 | Sugiyama | EBNA1BP2 EBP2 | NQKFGFGGKKKGSKWNtREsyDDVssFRAKTAHGRGLKRPG |
| Q99877 | Y41 | Sugiyama | H2BC15 H2BFD HIST1H2BN | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q99877 | Y43 | Sugiyama | H2BC15 H2BFD HIST1H2BN | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q99879 | Y41 | Sugiyama | H2BC14 H2BFE HIST1H2BM | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q99879 | Y43 | Sugiyama | H2BC14 H2BFE HIST1H2BM | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q99880 | Y41 | Sugiyama | H2BC13 H2BFC HIST1H2BL | KAQKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMG |
| Q99880 | Y43 | Sugiyama | H2BC13 H2BFC HIST1H2BL | QKKDGKKRKRSRKEsysVyVyKVLKQVHPDTGIssKAMGIM |
| Q9BPX3 | Y929 | Sugiyama | NCAPG CAPG NYMEL3 | QDATLTTTTFQNEDEKNKEVyMtPLRGVKATQASKSTQLKT |
| Q9BQE3 | T225 | Sugiyama | TUBA1C TUBA6 | DNEAIYDICRRNLDIERPtytNLNRLIsQIVSsITASLRFD |
| Q9BQE3 | Y103 | Sugiyama | TUBA1C TUBA6 | yRQLFHPEQLItGKEDAANNyARGHYTIGKEIIDLVLDRIR |
| Q9BQE3 | Y432 | Sugiyama | TUBA1C TUBA6 | GMEEGEFSEAREDMAALEKDyEEVGADsADGEDEGEEy___ |
| Q9BQE3 | Y449 | Sugiyama | TUBA1C TUBA6 | EKDyEEVGADsADGEDEGEEy____________________ |
| Q9BRK5 | Y342 | Sugiyama | SDF4 CAB45 PSEC0034 | MIAVADENQNHHLEPEEVLKysEFFTGSKLVDYARsVHEEF |
| Q9BS26 | S393 | Sugiyama | ERP44 KIAA0573 TXNDC4 UNQ532/PRO1075 | EQAQDVASSPPESSFQKLAPsEyRytLLRDRDEL_______ |
| Q9BS26 | Y397 | Sugiyama | ERP44 KIAA0573 TXNDC4 UNQ532/PRO1075 | DVASSPPESSFQKLAPsEyRytLLRDRDEL___________ |
| Q9BS40 | Y20 | Sugiyama | LXN | _MEIPPTNYPASRAALVAQNyINyQQGTPHRVFEVQKVKQA |
| Q9BS40 | Y23 | Sugiyama | LXN | IPPTNYPASRAALVAQNyINyQQGTPHRVFEVQKVKQAsME |
| Q9BVA1 | T107 | Sugiyama | TUBB2B | PDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKESESC |
| Q9BVA1 | Y106 | Sugiyama | TUBB2B | RPDNFVFGQsGAGNNWAKGHytEGAELVDsVLDVVRKESES |
| Q9BVP2 | Y542 | Sugiyama | GNL3 E2IG3 NS | AGEQSTRSFILDKIIEEDDAyDFSTDyV_____________ |
| Q9BVP2 | Y548 | Sugiyama | GNL3 E2IG3 NS | RSFILDKIIEEDDAyDFSTDyV___________________ |
| Q9BWF3 | Y194 | Sugiyama | RBM4 RBM4A | ECPIDRSGRVADLTEQYNEQyGAVRTPYTMSYGDSLYYNNA |
| Q9BX40 | Y311 | Sugiyama | LSM14B C20orf40 FAM61B RAP55B | AVVTQSAEAPAEEDLLGPNCyyDKSKSFFDNIssELKTSSR |
| Q9BX40 | Y312 | Sugiyama | LSM14B C20orf40 FAM61B RAP55B | VVTQSAEAPAEEDLLGPNCyyDKSKSFFDNIssELKTSSRR |
| Q9BYX7 | S239 | Sugiyama | POTEKP ACTBL3 FKSG30 | VALDSEQEMAMAASSSSVEKsyELPDGQVItIGNERFRCPE |
| Q9BYX7 | Y240 | Sugiyama | POTEKP ACTBL3 FKSG30 | ALDSEQEMAMAASSSSVEKsyELPDGQVItIGNERFRCPEA |
| Q9BYX7 | Y362 | Sugiyama | POTEKP ACTBL3 FKSG30 | GGSILASLSTFQQMWISKQEyDEsGPsIVHRKCF_______ |
| Q9BYX7 | Y91 | Sugiyama | POTEKP ACTBL3 FKSG30 | MEHGIITNWDDMEKIWHHtFyNELRVAPEEHPILLTEAPLN |
| Q9BZI7 | S166 | Sugiyama | UPF3B RENT3B UPF3X | KRDTKVGtIDDDPEyRKFLEsyAtDNEKMTstPEtLLEEIE |
| Q9GZY6 | Y110 | GPS6|EPSD|PSP | LAT2 LAB NTAL WBS15 WBSCR15 WBSCR5 HSPC046 | PASSRyQNFSKGsRHGsEEAyIDPIAMEyyNWGRFSKPPED |
| Q9GZY6 | Y118 | GPS6|EPSD|PSP | LAT2 LAB NTAL WBS15 WBSCR15 WBSCR5 HSPC046 | FSKGsRHGsEEAyIDPIAMEyyNWGRFSKPPEDDDANsyEN |
| Q9GZY6 | Y119 | GPS6|EPSD|PSP | LAT2 LAB NTAL WBS15 WBSCR15 WBSCR5 HSPC046 | SKGsRHGsEEAyIDPIAMEyyNWGRFSKPPEDDDANsyENV |
| Q9GZY6 | Y136 | GPS6|EPSD|PSP | LAT2 LAB NTAL WBS15 WBSCR15 WBSCR5 HSPC046 | MEyyNWGRFSKPPEDDDANsyENVLICKQKTTETGAQQEGI |
| Q9GZY6 | Y95 | GPS6|EPSD|PSP | LAT2 LAB NTAL WBS15 WBSCR15 WBSCR5 HSPC046 | TRKDKLLQFyPsLEDPASSRyQNFSKGsRHGsEEAyIDPIA |
| Q9H1E3 | Y146 | Sugiyama | NUCKS1 NUCKS JC7 | QEKDsGsDEDFLMEDDDDsDyGSsKKKNKKMVKKSKPERKE |
| Q9H2H8 | Y75 | Sugiyama | PPIL3 | DPTGTGRGGNSIWGKKFEDEysEyLKHNVRGVVSMANNGPN |
| Q9H2H8 | Y78 | Sugiyama | PPIL3 | GTGRGGNSIWGKKFEDEysEyLKHNVRGVVSMANNGPNTNG |
| Q9H3G5 | Y199 | Sugiyama | CPVL VLP PSEC0124 UNQ197/PRO223 | LYSALIQFFQIFPEYKNNDFyVTGESyAGKYVPAIAHLIHS |
| Q9H4M9 | Y339 | Sugiyama | EHD1 PAST PAST1 CDABP0131 | PNVFGKESKKKELVNNLGEIyQKIEREHQIsPGDFPsLRKM |
| Q9H6T3 | Y90 | Sugiyama | RPAP3 | KESSKKTREENTKNRIKsyDyEAWAKLDVDRILDELDKDDs |
| Q9H792 | Y635 | EPSD|PSP | PEAK1 KIAA2002 | tyARSSKNAIKVPIVINPNAyDNLAIyKSFLGtsGELSVKE |
| Q9H7Z7 | Y308 | Sugiyama | PTGES2 C9orf15 PGES2 | LISKRLKSRHRLQDNVREDLyEAADKWVAAVGKDRPFMGGQ |
| Q9H814 | Y154 | Sugiyama | PHAX RNUXA | LGILGMEGTIDRsRQsEtyNyLLAKKLRKESQEHTKDLDKE |
| Q9HAP6 | S115 | Sugiyama | LIN7B MALS2 VELI2 UNQ3116/PRO10200 | ELPKTDEGLGFNIMGGKEQNsPIyIsRVIPGGVADRHGGLK |
| Q9HAP6 | Y118 | Sugiyama | LIN7B MALS2 VELI2 UNQ3116/PRO10200 | KTDEGLGFNIMGGKEQNsPIyIsRVIPGGVADRHGGLKRGD |
| Q9HB07 | Y189 | Sugiyama | MYG1 C12orf10 | VEEVDAVDNGISQWAEGEPRyALttTLsARVARLNPTWNHP |
| Q9HBA0 | Y253 | GPS6|ELM|iPTMNet|EPSD | TRPV4 VRL2 VROAC | DIYYRGQTALHIAIERRCKHyVELLVAQGADVHAQARGRFF |
| Q9HC35 | T554 | Sugiyama | EML4 C2orf2 EMAPL4 | ILWDHDLNPEREIEVPDQyGtIRAVAEGKADQFLVGTSRNF |
| Q9HCN8 | Y81 | Sugiyama | SDF2L1 UNQ1941/PRO4424 | GSGSGQQSVtGVEAsDDANSyWRIRGGSEGGCPRGSPVRCG |
| Q9HDC5 | Y417 | Sugiyama | JPH1 JP1 | AARQECDIARAVARELsPDFyQPGPDyVKQRFQEGVDAKEN |
| Q9NQZ2 | T412 | Sugiyama | UTP3 CRLZ1 SAS10 | KEENstEEQALEDQNAKRAItyQIAKNRGLTPRRKKIDRNP |
| Q9NR46 | Y77 | Sugiyama | SH3GLB2 KIAA1848 PP578 | LRQTEVLLQPNPSARVEEFLyEKLDRKVPSRVTNGELLAQY |
| Q9NRX4 | Y57 | Sugiyama | PHPT1 PHP14 CGI-202 HSPC141 | AAESKEIVRGYKWAEyHADIyDKVSGDMQKQGCDCECLGGG |
| Q9NUL3 | Y326 | Sugiyama | STAU2 | MNPISRLAQIQQAKKEKEPDyVLLSERGMPRRREFVMQVKV |
| Q9NUP9 | S115 | Sugiyama | LIN7C MALS3 VELI3 | ELPKTEEGLGFNIMGGKEQNsPIyIsRIIPGGIADRHGGLK |
| Q9NUP9 | Y118 | Sugiyama | LIN7C MALS3 VELI3 | KTEEGLGFNIMGGKEQNsPIyIsRIIPGGIADRHGGLKRGD |
| Q9NVS9 | Y256 | Sugiyama | PNPO | LPtGDsPLGPMTHRGEEDWLyERLAP_______________ |
| Q9NWQ8 | Y317 | GPS6|SIGNOR | PAG1 CBP PAG | LsyKsREEDPTLTEEEIsAMyssVNKPGQLVNKsGQsLTVP |
| Q9NWQ8 | Y387 | SIGNOR | PAG1 CBP PAG | KTPNSTLPPAGRPSEEPEPDyEAIQtLNREEEKATLGTNGH |
| Q9NWQ8 | Y417 | SIGNOR | PAG1 CBP PAG | EEKATLGTNGHHGLVPKENDyEsISDLQQGRDITRL_____ |
| Q9NWS0 | Y194 | Sugiyama | PIH1D1 NOP17 | IsQQNIRSEQRPRIQELGDLytPAPGRAESGPEKPHLNLWL |
| Q9NX18 | Y105 | Sugiyama | SDHAF2 C11orf79 PGL2 SDH5 | LLSLFAKEHLQHMTEKQLNLyDRLINEPSNDWDIYYWATEA |
| Q9NX40 | Y199 | Sugiyama | OCIAD1 ASRIJ OCIA | HIVQGPDPNLEEsPKRKNITyEELRNKNREsyEVSLTQKTD |
| Q9NXV6 | T114 | Sugiyama | CDKN2AIP CARF | QKVMDKILSMAEGIKVtDAPtyTTRDELVAKVKKRGIsssN |
| Q9NXV6 | Y115 | Sugiyama | CDKN2AIP CARF | KVMDKILSMAEGIKVtDAPtyTTRDELVAKVKKRGIsssNE |
| Q9NY65 | T225 | Sugiyama | TUBA8 TUBAL2 | DNEAIYDICRRNLDIERPtytNLNRLIsQIVSsITASLRFD |
| Q9NY65 | Y103 | Sugiyama | TUBA8 TUBAL2 | YRQLFHPEQLItGKEDAANNyARGHYTVGKESIDLVLDRIR |
| Q9NYF8 | Y219 | Sugiyama | BCLAF1 BTF KIAA0164 | IDEFNKssAtsGDIWPGLsAyDNsPRsPHsPsPIAtPPSQS |
| Q9P0P0 | Y152 | Sugiyama | RNF181 HSPC238 | RDKARKQQQQHRLENLHGAMyt___________________ |
| Q9UBB9 | Y51 | Sugiyama | TFIP11 STIP HSPC006 | LQNEFNPNRQRHWQTKEEAtyGVWAERDsDDERPSFGGKRA |
| Q9UBQ7 | Y255 | Sugiyama | GRHPR GLXR MSTP035 | KETAVFINISRGDVVNQDDLyQALAsGKIAAAGLDVtsPEP |
| Q9UBR2 | Y76 | Sugiyama | CTSZ | YLSPADLPKSWDWRNVDGVNyAsItRNQHIPQYCGSCWAHA |
| Q9UBS4 | Y352 | Sugiyama | DNAJB11 EDJ ERJ3 HDJ9 PSEC0121 UNQ537/PRO1080 | TEEAREGIKQLLKQGSVQKVyNGLQGY______________ |
| Q9UBS4 | Y74 | Sugiyama | DNAJB11 EDJ ERJ3 HDJ9 PSEC0121 UNQ537/PRO1080 | PDRNPDDPQAQEKFQDLGAAyEVLsDSEKRKQyDTyGEEGL |
| Q9UDY4 | Y172 | Sugiyama | DNAJB4 DNAJW HLJ1 | SRLKQDPPVIHELRVsLEEIySGCTKRMKISRKRLNADGRS |
| Q9UGI8 | Y251 | Sugiyama | TES | RTQYSCYCCKLSMKEGDPAIyAERAGyDKLWHPACFVCSTC |
| Q9UHI6 | Y659 | Sugiyama | DDX20 DP103 GEMIN3 | RVPVLASSsQsGDsEsDSDSySSRTSSQSKGNKsyLEGssD |
| Q9UHR4 | Y380 | Sugiyama | BAIAP2L1 IRTKS | SFAQGDVITLLIPEEKDGWLyGEHDVSKARGWFPssYTKLL |
| Q9UI15 | Y192 | Sugiyama | TAGLN3 NP25 | NVIGLQMGSNKGAsQAGMtGyGMPRQIM_____________ |
| Q9UK17 | Y108 | SIGNOR | KCND3 | PEVFRCVLNFYRTGKLHYPRyECISAYDDELAFYGILPEII |
| Q9UK59 | Y533 | Sugiyama | DBR1 | LsDEHEPEQRKKIKRRNQAIyAAVDDDDDDAA_________ |
| Q9UKF6 | Y677 | Sugiyama | CPSF3 CPSF73 | EGsEDDESLREMVELAAQRLyEALtPVH_____________ |
| Q9UKK9 | Y198 | Sugiyama | NUDT5 NUDIX5 HSPC115 | LLQRLDALVAEEHLTVDARVySyALALKHANAKPFEVPFLK |
| Q9UKS6 | Y206 | Sugiyama | PACSIN3 | RKLQERVERCAKEAEKTKAQyEQtLAELHRYTPRYMEDMEQ |
| Q9UKY7 | Y95 | Sugiyama | CDV3 H41 | TKAVTKDEDEWKELEQKEVDysGLRVQAMQIssEKEEDDNE |
| Q9UMS0 | Y194 | Sugiyama | NFU1 HIRIP5 CGI-33 | KELLDTRIRPTVQEDGGDVIyKGFEDGIVQLKLQGSCTSCP |
| Q9UMX5 | Y65 | Sugiyama | NENF CIR2 SPUF | RLFtEEELARYGGEEEDQPIyLAVKGVVFDVtSGKEFYGRG |
| Q9UN19 | Y139 | SIGNOR|iPTMNet|EPSD|PSP | DAPP1 BAM32 HSPC066 | tGtLMVLKHPYPRKVEEPsIyEsVRVHTAMQTGRTEDDLVP |
| Q9UN86 | T21 | Sugiyama | G3BP2 KIAA0660 | MVMEKPsPLLVGREFVRQyytLLNKAPEYLHRFYGRNSSYV |
| Q9UN86 | Y19 | Sugiyama | G3BP2 KIAA0660 | __MVMEKPsPLLVGREFVRQyytLLNKAPEYLHRFYGRNSS |
| Q9UNZ2 | Y167 | Sugiyama | NSFL1C UBXN2C | PRPFAGGGYRLGAAPEEEsAyVAGEKRQHssQDVHVVLKLW |
| Q9UQ35 | Y2693 | Sugiyama | SRRM2 KIAA0324 SRL300 SRM300 HSPC075 | RRSRSPRKPIDsLRDsRsLsysPVERRRPsPQPsPRDQQSS |
| Q9UQ80 | Y343 | Sugiyama | PA2G4 EBP1 | VLLMPNGPMRITsGPFEPDLyKsEMEVQDAELKALLQssAs |
| Q9UQ80 | Y98 | Sugiyama | PA2G4 EBP1 | TSISVNNCVCHFsPLKSDQDyILKEGDLVKIDLGVHVDGFI |
| Q9UQE7 | Y225 | Sugiyama | SMC3 BAM BMH CSPG6 SMC3L1 | EEKEELAQYQKWDKMRRALEyTIyNQELNETRAKLDELSAK |
| Q9UQE7 | Y228 | Sugiyama | SMC3 BAM BMH CSPG6 SMC3L1 | EELAQYQKWDKMRRALEyTIyNQELNETRAKLDELSAKRET |
| Q9Y230 | Y172 | Sugiyama | RUVBL2 INO80J TIP48 TIP49B CGI-46 | TGTGSKVGKLTLKTTEMETIyDLGTKMIESLTKDKVQAGDV |
| Q9Y262 | Y409 | Sugiyama | EIF3L EIF3EIP EIF3S6IP HSPC021 HSPC025 MSTP005 | QLREKYGDKMLRMQKGDPQVyEELFsysCPKFLSPVVPNYD |
| Q9Y262 | Y415 | Sugiyama | EIF3L EIF3EIP EIF3S6IP HSPC021 HSPC025 MSTP005 | GDKMLRMQKGDPQVyEELFsysCPKFLSPVVPNYDNVHPNY |
| Q9Y262 | Y89 | Sugiyama | EIF3L EIF3EIP EIF3S6IP HSPC021 HSPC025 MSTP005 | QKVYELQASRVssDVIDQKVyEIQDIyENSWTKLTERFFKN |
| Q9Y262 | Y95 | Sugiyama | EIF3L EIF3EIP EIF3S6IP HSPC021 HSPC025 MSTP005 | QASRVssDVIDQKVyEIQDIyENSWTKLTERFFKNTPWPEA |
| Q9Y265 | Y438 | Sugiyama | RUVBL1 INO80H NMP238 TIP49 TIP49A | KINGKDSIEKEHVEEIsELFyDAKSSAKILADQQDKYMK__ |
| Q9Y281 | Y82 | Sugiyama | CFL2 | DTVEDPYtsFVKLLPLNDCRyALyDAtyEtKESKKEDLVFI |
| Q9Y281 | Y85 | Sugiyama | CFL2 | EDPYtsFVKLLPLNDCRyALyDAtyEtKESKKEDLVFIFWA |
| Q9Y281 | Y89 | Sugiyama | CFL2 | tsFVKLLPLNDCRyALyDAtyEtKESKKEDLVFIFWAPESA |
| Q9Y2B0 | Y71 | Sugiyama | CNPY2 MSAP TMEM4 ZSIG9 UNQ1943/PRO4426 | IQMGsFRINPDGsQsVVEVPyARsEAHLtELLEEICDRMKE |
| Q9Y2B0 | Y92 | Sugiyama | CNPY2 MSAP TMEM4 ZSIG9 UNQ1943/PRO4426 | ARsEAHLtELLEEICDRMKEyGEQIDPstHRKNYVRVVGRN |
| Q9Y2W1 | Y228 | Sugiyama | THRAP3 BCLAF2 TRAP150 | GGtsQDTKAsEssKPWPDAtyGtGsAsRAsAVsELsPRERs |
| Q9Y2W2 | Y236 | Sugiyama | WBP11 NPWBP SIPP1 SNP70 | GRKVGFALDLPPRRRDEDMLysPELAQRGHDDDVSSTSEDD |
| Q9Y3C1 | Y118 | Sugiyama | NOP16 CGI-117 HSPC111 | EAEASLPEKKGNTLSRDLIDyVRYMVENHGEDYKAMARDEK |
| Q9Y3F4 | Y300 | Sugiyama | STRAP MAWD UNRIP | yAsGSEDGTLRLWQTVVGKtyGLWKCVLPEEDsGELAKPKI |
| Q9Y3U8 | Y53 | Sugiyama | RPL36 | LTKHTKFVRDMIREVCGFAPyERRAMELLKVSKDKRALKFI |
| Q9Y490 | Y1893 | Sugiyama | TLN1 KIAA1027 TLN | TKsNtsPEELGPLANQLTsDyGRLAsEAKPAAVAAENEEIG |
| Q9Y5S9 | Y54 | Sugiyama | RBM8A RBM8 HSPC114 MDS014 | KRKGRGFGsEEGsRARMREDyDsVEQDGDEPGPQRSVEGWI |
| Q9Y5S9 | Y96 | Sugiyama | RBM8A RBM8 HSPC114 MDS014 | FVTGVHEEATEEDIHDKFAEyGEIKNIHLNLDRRTGYLKGy |
| Q9Y639 | Y216 | Sugiyama | NPTN SDFR1 SDR1 | KNASNMEYRINKPRAEDsGEyHCVyHFVsAPKANATIEVKA |
| Q9Y639 | Y220 | Sugiyama | NPTN SDFR1 SDR1 | NMEYRINKPRAEDsGEyHCVyHFVsAPKANATIEVKAAPDI |
| Q9Y696 | Y244 | Sugiyama | CLIC4 | AysRDEFtNtCPsDKEVEIAysDVAKRLTK___________ |
| Q9Y6K9 | Y374 | SIGNOR|PSP | IKBKG FIP3 NEMO | EDMRKRHVEVSQAPLPPAPAyLssPLALPsQRRsPPEEPPD |
| Q9Y6L6 | Y645 | PSP | SLCO1B1 LST1 OATP1B1 OATP2 OATPC SLC21A6 | YLGLSSMLRVSSLVLyIILIyAMKKKYQEKDINASENGSVM |
| Q9Y6Y9 | Y131 | EPSD|PSP | LY96 ESOP1 MD2 | ETVNTTISFSFKGIKFSKGKyKCVVEAISGSPEEMLFCLEF |
| Q9Y6Y9 | Y22 | EPSD|PSP | LY96 ESOP1 MD2 | LPFLFFSTLFSSIFTEAQKQyWVCNSSDASISYTYCDKMQY |
Site Promiscuity
Motif of predicted substrate sequence
Reactome pathways of predicted substrates
Download
| name | reactome_id | p | -log10p | ref_path | ref_path_lowest |
|---|---|---|---|---|---|
| Axon guidance | R-HSA-422475 | 7.829314e-10 | 9.106 | 1 | 0 |
| Nervous system development | R-HSA-9675108 | 2.889195e-09 | 8.539 | 1 | 0 |
| Fcgamma receptor (FCGR) dependent phagocytosis | R-HSA-2029480 | 2.718879e-07 | 6.566 | 1 | 0 |
| GPVI-mediated activation cascade | R-HSA-114604 | 6.004519e-07 | 6.222 | 1 | 1 |
| Hemostasis | R-HSA-109582 | 8.156575e-07 | 6.088 | 1 | 0 |
| VEGFA-VEGFR2 Pathway | R-HSA-4420097 | 1.972295e-06 | 5.705 | 0 | 0 |
| Signaling by Receptor Tyrosine Kinases | R-HSA-9006934 | 1.994657e-06 | 5.700 | 1 | 0 |
| Signaling by VEGF | R-HSA-194138 | 4.034274e-06 | 5.394 | 0 | 0 |
| Platelet activation, signaling and aggregation | R-HSA-76002 | 5.316736e-06 | 5.274 | 1 | 0 |
| Cell-Cell communication | R-HSA-1500931 | 5.243604e-06 | 5.280 | 0 | 0 |
| Immune System | R-HSA-168256 | 4.828879e-06 | 5.316 | 1 | 0 |
| Developmental Biology | R-HSA-1266738 | 6.177470e-06 | 5.209 | 1 | 0 |
| Regulation of signaling by CBL | R-HSA-912631 | 7.906866e-06 | 5.102 | 1 | 1 |
| Receptor Mediated Mitophagy | R-HSA-8934903 | 1.468703e-05 | 4.833 | 0 | 0 |
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | R-HSA-9670439 | 1.649864e-05 | 4.783 | 1 | 1 |
| Selective autophagy | R-HSA-9663891 | 1.374057e-05 | 4.862 | 0 | 0 |
| Signaling by KIT in disease | R-HSA-9669938 | 1.649864e-05 | 4.783 | 1 | 0 |
| Signal Transduction | R-HSA-162582 | 1.487378e-05 | 4.828 | 1 | 0 |
| PECAM1 interactions | R-HSA-210990 | 1.958742e-05 | 4.708 | 1 | 1 |
| EPH-Ephrin signaling | R-HSA-2682334 | 1.961717e-05 | 4.707 | 1 | 1 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | R-HSA-512988 | 2.162285e-05 | 4.665 | 1 | 0 |
| Signaling by SCF-KIT | R-HSA-1433557 | 2.413307e-05 | 4.617 | 1 | 1 |
| EPH-ephrin mediated repulsion of cells | R-HSA-3928665 | 3.662421e-05 | 4.436 | 1 | 1 |
| Co-stimulation by CD28 | R-HSA-389356 | 4.044101e-05 | 4.393 | 1 | 1 |
| DAP12 signaling | R-HSA-2424491 | 5.402931e-05 | 4.267 | 0 | 0 |
| Sema3A PAK dependent Axon repulsion | R-HSA-399954 | 6.368237e-05 | 4.196 | 0 | 0 |
| Innate Immune System | R-HSA-168249 | 6.509858e-05 | 4.186 | 1 | 0 |
| Mitophagy | R-HSA-5205647 | 9.907758e-05 | 4.004 | 0 | 0 |
| Autophagy | R-HSA-9612973 | 1.445207e-04 | 3.840 | 0 | 0 |
| Semaphorin interactions | R-HSA-373755 | 1.468396e-04 | 3.833 | 0 | 0 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | R-HSA-6811558 | 1.506150e-04 | 3.822 | 0 | 0 |
| Constitutive Signaling by Aberrant PI3K in Cancer | R-HSA-2219530 | 1.667130e-04 | 3.778 | 0 | 0 |
| Interleukin-2 family signaling | R-HSA-451927 | 1.860804e-04 | 3.730 | 0 | 0 |
| Role of ABL in ROBO-SLIT signaling | R-HSA-428890 | 1.973881e-04 | 3.705 | 0 | 0 |
| VEGFR2 mediated vascular permeability | R-HSA-5218920 | 2.049335e-04 | 3.688 | 0 | 0 |
| Negative regulation of the PI3K/AKT network | R-HSA-199418 | 2.203793e-04 | 3.657 | 0 | 0 |
| Regulation of T cell activation by CD28 family | R-HSA-388841 | 2.582230e-04 | 3.588 | 1 | 0 |
| Recruitment of mitotic centrosome proteins and complexes | R-HSA-380270 | 2.960388e-04 | 3.529 | 0 | 0 |
| DAP12 interactions | R-HSA-2172127 | 2.952666e-04 | 3.530 | 0 | 0 |
| EPHB-mediated forward signaling | R-HSA-3928662 | 2.952666e-04 | 3.530 | 1 | 1 |
| Diseases of signal transduction by growth factor receptors and second messengers | R-HSA-5663202 | 2.957115e-04 | 3.529 | 1 | 0 |
| Centrosome maturation | R-HSA-380287 | 3.366231e-04 | 3.473 | 0 | 0 |
| Parasite infection | R-HSA-9664407 | 3.729529e-04 | 3.428 | 1 | 0 |
| Leishmania phagocytosis | R-HSA-9664417 | 3.729529e-04 | 3.428 | 1 | 0 |
| FCGR3A-mediated phagocytosis | R-HSA-9664422 | 3.729529e-04 | 3.428 | 1 | 1 |
| Regulation of actin dynamics for phagocytic cup formation | R-HSA-2029482 | 3.888080e-04 | 3.410 | 0 | 0 |
| Macroautophagy | R-HSA-1632852 | 3.888080e-04 | 3.410 | 0 | 0 |
| G alpha (12/13) signalling events | R-HSA-416482 | 4.055331e-04 | 3.392 | 0 | 0 |
| Cytokine Signaling in Immune system | R-HSA-1280215 | 3.935431e-04 | 3.405 | 1 | 0 |
| G2/M Transition | R-HSA-69275 | 4.746833e-04 | 3.324 | 0 | 0 |
| Mitotic G2-G2/M phases | R-HSA-453274 | 5.085557e-04 | 3.294 | 0 | 0 |
| EPHA-mediated growth cone collapse | R-HSA-3928663 | 5.146720e-04 | 3.288 | 1 | 1 |
| Condensation of Prometaphase Chromosomes | R-HSA-2514853 | 6.400387e-04 | 3.194 | 0 | 0 |
| Regulation of gene expression in beta cells | R-HSA-210745 | 6.403315e-04 | 3.194 | 0 | 0 |
| Downstream signal transduction | R-HSA-186763 | 7.863257e-04 | 3.104 | 0 | 0 |
| Phosphorylation and nuclear translocation of the CRY:PER:kinase complex | R-HSA-9931530 | 7.705840e-04 | 3.113 | 0 | 0 |
| NRAGE signals death through JNK | R-HSA-193648 | 7.508519e-04 | 3.124 | 0 | 0 |
| Signaling by Interleukins | R-HSA-449147 | 7.904355e-04 | 3.102 | 1 | 0 |
| Intracellular signaling by second messengers | R-HSA-9006925 | 7.004434e-04 | 3.155 | 0 | 0 |
| PIP3 activates AKT signaling | R-HSA-1257604 | 7.682634e-04 | 3.114 | 0 | 0 |
| PI3K/AKT Signaling in Cancer | R-HSA-2219528 | 6.862839e-04 | 3.163 | 0 | 0 |
| Neutrophil degranulation | R-HSA-6798695 | 8.499124e-04 | 3.071 | 0 | 0 |
| RUNX3 regulates RUNX1-mediated transcription | R-HSA-8951911 | 9.232824e-04 | 3.035 | 0 | 0 |
| Signaling by ERBB2 | R-HSA-1227986 | 9.818532e-04 | 3.008 | 0 | 0 |
| Regulation of CDH1 posttranslational processing and trafficking to plasma membrane | R-HSA-9768727 | 1.047223e-03 | 2.980 | 0 | 0 |
| Signal regulatory protein family interactions | R-HSA-391160 | 1.079787e-03 | 2.967 | 0 | 0 |
| Regulation of KIT signaling | R-HSA-1433559 | 1.079787e-03 | 2.967 | 1 | 1 |
| Signaling by CSF1 (M-CSF) in myeloid cells | R-HSA-9680350 | 1.146229e-03 | 2.941 | 1 | 1 |
| NPAS4 regulates expression of target genes | R-HSA-9768919 | 1.146229e-03 | 2.941 | 0 | 0 |
| DCC mediated attractive signaling | R-HSA-418885 | 1.259836e-03 | 2.900 | 0 | 0 |
| RET signaling | R-HSA-8853659 | 1.363602e-03 | 2.865 | 0 | 0 |
| Kidney development | R-HSA-9830369 | 1.507741e-03 | 2.822 | 0 | 0 |
| Respiratory Syncytial Virus Infection Pathway | R-HSA-9820952 | 1.654975e-03 | 2.781 | 0 | 0 |
| Signaling by ALK | R-HSA-201556 | 1.741290e-03 | 2.759 | 0 | 0 |
| Cell junction organization | R-HSA-446728 | 1.773420e-03 | 2.751 | 0 | 0 |
| Parasitic Infection Pathways | R-HSA-9824443 | 1.906605e-03 | 2.720 | 1 | 0 |
| Leishmania infection | R-HSA-9658195 | 1.906605e-03 | 2.720 | 1 | 0 |
| Response of endothelial cells to shear stress | R-HSA-9860931 | 1.790681e-03 | 2.747 | 0 | 0 |
| Respiratory syncytial virus (RSV) genome replication, transcription and translation | R-HSA-9820965 | 1.741290e-03 | 2.759 | 0 | 0 |
| Cell death signalling via NRAGE, NRIF and NADE | R-HSA-204998 | 2.102727e-03 | 2.677 | 0 | 0 |
| Chaperone Mediated Autophagy | R-HSA-9613829 | 2.164643e-03 | 2.665 | 0 | 0 |
| Cell surface interactions at the vascular wall | R-HSA-202733 | 2.249477e-03 | 2.648 | 1 | 1 |
| Reelin signalling pathway | R-HSA-8866376 | 2.767384e-03 | 2.558 | 0 | 0 |
| Phosphorylation and nuclear translocation of BMAL1 (ARNTL) and CLOCK | R-HSA-9931529 | 2.767384e-03 | 2.558 | 0 | 0 |
| Co-inhibition by CTLA4 | R-HSA-389513 | 2.735950e-03 | 2.563 | 1 | 1 |
| Regulation of MITF-M dependent genes involved in invasion | R-HSA-9854909 | 2.767384e-03 | 2.558 | 0 | 0 |
| Signal transduction by L1 | R-HSA-445144 | 2.735950e-03 | 2.563 | 0 | 0 |
| Cellular responses to mechanical stimuli | R-HSA-9855142 | 2.809624e-03 | 2.551 | 0 | 0 |
| High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells | R-HSA-9856530 | 2.994844e-03 | 2.524 | 0 | 0 |
| Cell-cell junction organization | R-HSA-421270 | 3.188484e-03 | 2.496 | 0 | 0 |
| Adaptive Immune System | R-HSA-1280218 | 3.192576e-03 | 2.496 | 1 | 0 |
| Regulation of PLK1 Activity at G2/M Transition | R-HSA-2565942 | 3.612742e-03 | 2.442 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in cell cycle and proliferation | R-HSA-9825892 | 3.392127e-03 | 2.470 | 0 | 0 |
| Transcriptional regulation by RUNX2 | R-HSA-8878166 | 3.652539e-03 | 2.437 | 0 | 0 |
| Interleukin receptor SHC signaling | R-HSA-912526 | 4.136896e-03 | 2.383 | 0 | 0 |
| Transcriptional Regulation by NPAS4 | R-HSA-9634815 | 4.481091e-03 | 2.349 | 0 | 0 |
| Nef and signal transduction | R-HSA-164944 | 4.509667e-03 | 2.346 | 0 | 0 |
| Regulation of RUNX1 Expression and Activity | R-HSA-8934593 | 5.427428e-03 | 2.265 | 0 | 0 |
| Cell Cycle, Mitotic | R-HSA-69278 | 5.424975e-03 | 2.266 | 1 | 0 |
| Formation of the nephric duct | R-HSA-9830364 | 4.973623e-03 | 2.303 | 0 | 0 |
| Uptake and function of diphtheria toxin | R-HSA-5336415 | 5.527853e-03 | 2.257 | 0 | 0 |
| Regulation of Expression and Function of Type I Classical Cadherins | R-HSA-9764274 | 5.505028e-03 | 2.259 | 0 | 0 |
| Regulation of CDH1 Expression and Function | R-HSA-9764265 | 5.505028e-03 | 2.259 | 0 | 0 |
| Signaling by EGFR | R-HSA-177929 | 5.609916e-03 | 2.251 | 0 | 0 |
| Signaling by NTRK2 (TRKB) | R-HSA-9006115 | 5.905328e-03 | 2.229 | 0 | 0 |
| CD28 dependent PI3K/Akt signaling | R-HSA-389357 | 5.905328e-03 | 2.229 | 0 | 0 |
| RUNX2 regulates osteoblast differentiation | R-HSA-8940973 | 6.407653e-03 | 2.193 | 0 | 0 |
| Regulation of beta-cell development | R-HSA-186712 | 6.571169e-03 | 2.182 | 0 | 0 |
| Activated NTRK2 signals through FYN | R-HSA-9032500 | 6.641126e-03 | 2.178 | 0 | 0 |
| Co-stimulation by ICOS | R-HSA-9927354 | 6.641126e-03 | 2.178 | 0 | 0 |
| Loss of proteins required for interphase microtubule organization from the centrosome | R-HSA-380284 | 8.014406e-03 | 2.096 | 0 | 0 |
| Loss of Nlp from mitotic centrosomes | R-HSA-380259 | 8.014406e-03 | 2.096 | 0 | 0 |
| Signaling by PDGF | R-HSA-186797 | 7.635799e-03 | 2.117 | 0 | 0 |
| Transcriptional regulation by RUNX3 | R-HSA-8878159 | 7.013263e-03 | 2.154 | 0 | 0 |
| WNT mediated activation of DVL | R-HSA-201688 | 7.847320e-03 | 2.105 | 0 | 0 |
| Caspase-mediated cleavage of cytoskeletal proteins | R-HSA-264870 | 7.847320e-03 | 2.105 | 0 | 0 |
| Respiratory syncytial virus genome replication | R-HSA-9834752 | 7.847320e-03 | 2.105 | 0 | 0 |
| p75 NTR receptor-mediated signalling | R-HSA-193704 | 7.555627e-03 | 2.122 | 0 | 0 |
| MAPK1/MAPK3 signaling | R-HSA-5684996 | 8.416323e-03 | 2.075 | 0 | 0 |
| G0 and Early G1 | R-HSA-1538133 | 8.667050e-03 | 2.062 | 0 | 0 |
| Apoptotic cleavage of cellular proteins | R-HSA-111465 | 8.667050e-03 | 2.062 | 0 | 0 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | R-HSA-8950505 | 8.808149e-03 | 2.055 | 0 | 0 |
| Assembly and release of respiratory syncytial virus (RSV) virions | R-HSA-9820962 | 9.144308e-03 | 2.039 | 0 | 0 |
| AURKA Activation by TPX2 | R-HSA-8854518 | 9.223584e-03 | 2.035 | 0 | 0 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | R-HSA-8939243 | 9.295730e-03 | 2.032 | 0 | 0 |
| mRNA Splicing - Major Pathway | R-HSA-72163 | 9.432257e-03 | 2.025 | 0 | 0 |
| Regulation of Homotypic Cell-Cell Adhesion | R-HSA-9759476 | 9.891493e-03 | 2.005 | 0 | 0 |
| SARS-CoV-1-host interactions | R-HSA-9692914 | 1.001799e-02 | 1.999 | 0 | 0 |
| Drug resistance of ALK mutants | R-HSA-9700649 | 1.087046e-02 | 1.964 | 0 | 0 |
| Defective F9 secretion | R-HSA-9673218 | 1.087046e-02 | 1.964 | 0 | 0 |
| brigatinib-resistant ALK mutants | R-HSA-9717319 | 1.087046e-02 | 1.964 | 0 | 0 |
| alectinib-resistant ALK mutants | R-HSA-9717316 | 1.087046e-02 | 1.964 | 0 | 0 |
| NVP-TAE684-resistant ALK mutants | R-HSA-9717301 | 1.087046e-02 | 1.964 | 0 | 0 |
| ceritinib-resistant ALK mutants | R-HSA-9717323 | 1.087046e-02 | 1.964 | 0 | 0 |
| ASP-3026-resistant ALK mutants | R-HSA-9717264 | 1.087046e-02 | 1.964 | 0 | 0 |
| lorlatinib-resistant ALK mutants | R-HSA-9717329 | 1.087046e-02 | 1.964 | 0 | 0 |
| crizotinib-resistant ALK mutants | R-HSA-9717326 | 1.087046e-02 | 1.964 | 0 | 0 |
| InlA-mediated entry of Listeria monocytogenes into host cells | R-HSA-8876493 | 1.053000e-02 | 1.978 | 0 | 0 |
| Regulation of TBK1, IKKε (IKBKE)-mediated activation of IRF3, IRF7 | R-HSA-9824878 | 1.200232e-02 | 1.921 | 0 | 0 |
| HSF1 activation | R-HSA-3371511 | 1.207231e-02 | 1.918 | 0 | 0 |
| RUNX2 regulates bone development | R-HSA-8941326 | 1.207231e-02 | 1.918 | 0 | 0 |
| Death Receptor Signaling | R-HSA-73887 | 1.211283e-02 | 1.917 | 0 | 0 |
| mRNA Splicing | R-HSA-72172 | 1.216227e-02 | 1.915 | 0 | 0 |
| Ovarian tumor domain proteases | R-HSA-5689896 | 1.283280e-02 | 1.892 | 0 | 0 |
| Z-decay: degradation of maternal mRNAs by zygotically expressed factors | R-HSA-9820865 | 1.355927e-02 | 1.868 | 0 | 0 |
| Interleukin-12 signaling | R-HSA-9020591 | 1.409161e-02 | 1.851 | 0 | 0 |
| Cell Cycle | R-HSA-1640170 | 1.449322e-02 | 1.839 | 1 | 0 |
| CD28 dependent Vav1 pathway | R-HSA-389359 | 1.519884e-02 | 1.818 | 0 | 0 |
| Aggrephagy | R-HSA-9646399 | 1.527580e-02 | 1.816 | 0 | 0 |
| Adherens junctions interactions | R-HSA-418990 | 1.641016e-02 | 1.785 | 0 | 0 |
| CRMPs in Sema3A signaling | R-HSA-399956 | 1.691907e-02 | 1.772 | 0 | 0 |
| Activation and oligomerization of BAK protein | R-HSA-111452 | 2.162343e-02 | 1.665 | 0 | 0 |
| SARS-CoV-1 targets PDZ proteins in cell-cell junction | R-HSA-9692912 | 2.162343e-02 | 1.665 | 0 | 0 |
| Recruitment of NuMA to mitotic centrosomes | R-HSA-380320 | 2.249925e-02 | 1.648 | 0 | 0 |
| Activation of IRF3, IRF7 mediated by TBK1, IKKε (IKBKE) | R-HSA-936964 | 2.254465e-02 | 1.647 | 0 | 0 |
| IRF3-mediated induction of type I IFN | R-HSA-3270619 | 1.871804e-02 | 1.728 | 0 | 0 |
| Regulation of innate immune responses to cytosolic DNA | R-HSA-3134975 | 2.254465e-02 | 1.647 | 0 | 0 |
| TRAF3-dependent IRF activation pathway | R-HSA-918233 | 2.254465e-02 | 1.647 | 0 | 0 |
| FCGR3A-mediated IL10 synthesis | R-HSA-9664323 | 2.003398e-02 | 1.698 | 1 | 1 |
| Platelet degranulation | R-HSA-114608 | 2.057785e-02 | 1.687 | 0 | 0 |
| Netrin-1 signaling | R-HSA-373752 | 1.989159e-02 | 1.701 | 0 | 0 |
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | R-HSA-1362300 | 2.059386e-02 | 1.686 | 0 | 0 |
| Protein methylation | R-HSA-8876725 | 1.871804e-02 | 1.728 | 0 | 0 |
| Factors involved in megakaryocyte development and platelet production | R-HSA-983231 | 2.056567e-02 | 1.687 | 0 | 0 |
| RAF/MAP kinase cascade | R-HSA-5673001 | 2.111365e-02 | 1.675 | 0 | 0 |
| Regulation of TP53 Activity through Phosphorylation | R-HSA-6804756 | 2.104526e-02 | 1.677 | 0 | 0 |
| MAPK family signaling cascades | R-HSA-5683057 | 2.033247e-02 | 1.692 | 0 | 0 |
| G1 Phase | R-HSA-69236 | 1.989159e-02 | 1.701 | 1 | 0 |
| Cyclin D associated events in G1 | R-HSA-69231 | 1.989159e-02 | 1.701 | 1 | 1 |
| Apoptotic execution phase | R-HSA-75153 | 2.192975e-02 | 1.659 | 0 | 0 |
| SARS-CoV-1 Infection | R-HSA-9678108 | 2.056567e-02 | 1.687 | 0 | 0 |
| Interleukin-12 family signaling | R-HSA-447115 | 2.176480e-02 | 1.662 | 0 | 0 |
| Anchoring of the basal body to the plasma membrane | R-HSA-5620912 | 2.401313e-02 | 1.620 | 0 | 0 |
| Response to elevated platelet cytosolic Ca2+ | R-HSA-76005 | 2.465624e-02 | 1.608 | 0 | 0 |
| Degradation of CDH1 | R-HSA-9766229 | 2.519305e-02 | 1.599 | 0 | 0 |
| Azathioprine ADME | R-HSA-9748787 | 2.633573e-02 | 1.579 | 0 | 0 |
| Ephrin signaling | R-HSA-3928664 | 2.666388e-02 | 1.574 | 0 | 0 |
| GAB1 signalosome | R-HSA-180292 | 2.666388e-02 | 1.574 | 0 | 0 |
| Nephron development | R-HSA-9831926 | 2.666388e-02 | 1.574 | 0 | 0 |
| FCGR activation | R-HSA-2029481 | 2.722247e-02 | 1.565 | 1 | 1 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | R-HSA-983695 | 2.722247e-02 | 1.565 | 1 | 1 |
| SARS-CoV-1 activates/modulates innate immune responses | R-HSA-9692916 | 2.870325e-02 | 1.542 | 0 | 0 |
| STING mediated induction of host immune responses | R-HSA-1834941 | 2.882874e-02 | 1.540 | 0 | 0 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | R-HSA-168928 | 2.891876e-02 | 1.539 | 0 | 0 |
| Regulation of PTEN stability and activity | R-HSA-8948751 | 2.992800e-02 | 1.524 | 0 | 0 |
| Mitotic Prometaphase | R-HSA-68877 | 2.993225e-02 | 1.524 | 0 | 0 |
| Nephrin family interactions | R-HSA-373753 | 3.106144e-02 | 1.508 | 0 | 0 |
| Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG) | R-HSA-5660686 | 3.226015e-02 | 1.491 | 0 | 0 |
| Variant SLC6A20 contributes towards hyperglycinuria (HG) and iminoglycinuria (IG) | R-HSA-5619101 | 3.226015e-02 | 1.491 | 0 | 0 |
| Drug resistance in ERBB2 KD mutants | R-HSA-9665230 | 4.278188e-02 | 1.369 | 0 | 0 |
| Drug-mediated inhibition of ERBB2 signaling | R-HSA-9652282 | 4.278188e-02 | 1.369 | 0 | 0 |
| Resistance of ERBB2 KD mutants to afatinib | R-HSA-9665249 | 4.278188e-02 | 1.369 | 0 | 0 |
| Resistance of ERBB2 KD mutants to tesevatinib | R-HSA-9665245 | 4.278188e-02 | 1.369 | 0 | 0 |
| Resistance of ERBB2 KD mutants to neratinib | R-HSA-9665246 | 4.278188e-02 | 1.369 | 0 | 0 |
| Drug resistance in ERBB2 TMD/JMD mutants | R-HSA-9665737 | 4.278188e-02 | 1.369 | 0 | 0 |
| Resistance of ERBB2 KD mutants to lapatinib | R-HSA-9665251 | 4.278188e-02 | 1.369 | 0 | 0 |
| Defective F9 variant does not activate FX | R-HSA-9673202 | 4.278188e-02 | 1.369 | 0 | 0 |
| Resistance of ERBB2 KD mutants to trastuzumab | R-HSA-9665233 | 4.278188e-02 | 1.369 | 0 | 0 |
| Defective factor IX causes thrombophilia | R-HSA-9672383 | 4.278188e-02 | 1.369 | 0 | 0 |
| Resistance of ERBB2 KD mutants to sapitinib | R-HSA-9665244 | 4.278188e-02 | 1.369 | 0 | 0 |
| Resistance of ERBB2 KD mutants to osimertinib | R-HSA-9665247 | 4.278188e-02 | 1.369 | 0 | 0 |
| Defective cofactor function of FVIIIa variant | R-HSA-9672396 | 4.278188e-02 | 1.369 | 0 | 0 |
| Resistance of ERBB2 KD mutants to AEE788 | R-HSA-9665250 | 4.278188e-02 | 1.369 | 0 | 0 |
| Regulation of CDH1 Function | R-HSA-9764561 | 3.509873e-02 | 1.455 | 0 | 0 |
| Listeria monocytogenes entry into host cells | R-HSA-8876384 | 3.572351e-02 | 1.447 | 0 | 0 |
| Signaling by ALK in cancer | R-HSA-9700206 | 4.252849e-02 | 1.371 | 0 | 0 |
| Mitotic G1 phase and G1/S transition | R-HSA-453279 | 3.505602e-02 | 1.455 | 1 | 0 |
| Fc epsilon receptor (FCERI) signaling | R-HSA-2454202 | 3.618038e-02 | 1.442 | 1 | 1 |
| Signaling by ALK fusions and activated point mutants | R-HSA-9725370 | 4.252849e-02 | 1.371 | 0 | 0 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | R-HSA-8852276 | 4.216658e-02 | 1.375 | 0 | 0 |
| Extra-nuclear estrogen signaling | R-HSA-9009391 | 3.534221e-02 | 1.452 | 0 | 0 |
| Signaling by ROBO receptors | R-HSA-376176 | 3.618038e-02 | 1.442 | 0 | 0 |
| Signaling by NTRKs | R-HSA-166520 | 3.661924e-02 | 1.436 | 0 | 0 |
| The role of Nef in HIV-1 replication and disease pathogenesis | R-HSA-164952 | 4.063673e-02 | 1.391 | 0 | 0 |
| Potential therapeutics for SARS | R-HSA-9679191 | 3.822481e-02 | 1.418 | 0 | 0 |
| MITF-M-dependent gene expression | R-HSA-9856651 | 3.822481e-02 | 1.418 | 0 | 0 |
| Programmed Cell Death | R-HSA-5357801 | 3.820651e-02 | 1.418 | 0 | 0 |
| Deadenylation of mRNA | R-HSA-429947 | 4.318347e-02 | 1.365 | 0 | 0 |
| Signaling by ERBB2 TMD/JMD mutants | R-HSA-9665686 | 4.318347e-02 | 1.365 | 0 | 0 |
| Signaling by PTK6 | R-HSA-8848021 | 4.365960e-02 | 1.360 | 0 | 0 |
| Signaling by Non-Receptor Tyrosine Kinases | R-HSA-9006927 | 4.365960e-02 | 1.360 | 0 | 0 |
| Tight junction interactions | R-HSA-420029 | 4.578820e-02 | 1.339 | 0 | 0 |
| VEGFR2 mediated cell proliferation | R-HSA-5218921 | 4.578820e-02 | 1.339 | 0 | 0 |
| Interleukin-7 signaling | R-HSA-1266695 | 4.578820e-02 | 1.339 | 0 | 0 |
| TCR signaling | R-HSA-202403 | 4.584263e-02 | 1.339 | 0 | 0 |
| Regulation of TP53 Activity | R-HSA-5633007 | 4.689412e-02 | 1.329 | 0 | 0 |
| Processing of Capped Intron-Containing Pre-mRNA | R-HSA-72203 | 4.722880e-02 | 1.326 | 0 | 0 |
| FCERI mediated MAPK activation | R-HSA-2871796 | 4.813007e-02 | 1.318 | 1 | 1 |
| Myogenesis | R-HSA-525793 | 4.844936e-02 | 1.315 | 0 | 0 |
| Apoptosis | R-HSA-109581 | 4.875720e-02 | 1.312 | 0 | 0 |
| Phosphorylation of CD3 and TCR zeta chains | R-HSA-202427 | 5.116544e-02 | 1.291 | 0 | 0 |
| Maturation of hRSV A proteins | R-HSA-9828806 | 5.116544e-02 | 1.291 | 0 | 0 |
| Mitochondrial unfolded protein response (UPRmt) | R-HSA-9841251 | 5.116544e-02 | 1.291 | 0 | 0 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | R-HSA-3371497 | 5.151429e-02 | 1.288 | 0 | 0 |
| Defective gamma-carboxylation of F9 | R-HSA-9673240 | 5.318986e-02 | 1.274 | 0 | 0 |
| Defective ABCC2 causes DJS | R-HSA-5679001 | 5.318986e-02 | 1.274 | 0 | 0 |
| Defective CYP19A1 causes AEXS | R-HSA-5579030 | 5.318986e-02 | 1.274 | 0 | 0 |
| STAT6-mediated induction of chemokines | R-HSA-3249367 | 5.318986e-02 | 1.274 | 0 | 0 |
| Disease | R-HSA-1643685 | 5.383996e-02 | 1.269 | 1 | 0 |
| FCERI mediated Ca+2 mobilization | R-HSA-2871809 | 5.412072e-02 | 1.267 | 1 | 1 |
| Transcriptional regulation by RUNX1 | R-HSA-8878171 | 5.441236e-02 | 1.264 | 0 | 0 |
| Cytosolic sensors of pathogen-associated DNA | R-HSA-1834949 | 5.483497e-02 | 1.261 | 0 | 0 |
| L1CAM interactions | R-HSA-373760 | 5.536530e-02 | 1.257 | 0 | 0 |
| Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 complexes | R-HSA-69200 | 6.348530e-02 | 1.197 | 0 | 0 |
| GRB7 events in ERBB2 signaling | R-HSA-1306955 | 6.348530e-02 | 1.197 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in interleukin signaling | R-HSA-8939247 | 7.366943e-02 | 1.133 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in BCR signaling | R-HSA-8939245 | 7.366943e-02 | 1.133 | 0 | 0 |
| G2 Phase | R-HSA-68911 | 7.366943e-02 | 1.133 | 0 | 0 |
| NTRK2 activates RAC1 | R-HSA-9032759 | 7.366943e-02 | 1.133 | 0 | 0 |
| Defective F9 activation | R-HSA-9673221 | 7.366943e-02 | 1.133 | 0 | 0 |
| RUNX1 regulates expression of components of tight junctions | R-HSA-8935964 | 8.374343e-02 | 1.077 | 0 | 0 |
| CDH11 homotypic and heterotypic interactions | R-HSA-9833576 | 8.374343e-02 | 1.077 | 0 | 0 |
| PTK6 Regulates Cell Cycle | R-HSA-8849470 | 8.374343e-02 | 1.077 | 0 | 0 |
| Defective CSF2RB causes SMDP5 | R-HSA-5688849 | 8.374343e-02 | 1.077 | 0 | 0 |
| Defective CSF2RA causes SMDP4 | R-HSA-5688890 | 8.374343e-02 | 1.077 | 0 | 0 |
| Cyclin A/B1/B2 associated events during G2/M transition | R-HSA-69273 | 6.853332e-02 | 1.164 | 0 | 0 |
| LRR FLII-interacting protein 1 (LRRFIP1) activates type I IFN production | R-HSA-3134973 | 7.366943e-02 | 1.133 | 0 | 0 |
| Integrin signaling | R-HSA-354192 | 6.853332e-02 | 1.164 | 0 | 0 |
| Regulation of gap junction activity | R-HSA-191650 | 6.348530e-02 | 1.197 | 0 | 0 |
| MDK and PTN in ALK signaling | R-HSA-9851151 | 6.348530e-02 | 1.197 | 0 | 0 |
| IRF3 mediated activation of type 1 IFN | R-HSA-1606341 | 7.366943e-02 | 1.133 | 0 | 0 |
| Aryl hydrocarbon receptor signalling | R-HSA-8937144 | 8.374343e-02 | 1.077 | 0 | 0 |
| Signaling by ERBB2 KD Mutants | R-HSA-9664565 | 5.675640e-02 | 1.246 | 0 | 0 |
| Signaling by ERBB2 in Cancer | R-HSA-1227990 | 5.962837e-02 | 1.225 | 0 | 0 |
| Downregulation of ERBB2 signaling | R-HSA-8863795 | 5.962837e-02 | 1.225 | 0 | 0 |
| ISG15 antiviral mechanism | R-HSA-1169408 | 6.357120e-02 | 1.197 | 0 | 0 |
| Negative regulators of DDX58/IFIH1 signaling | R-HSA-936440 | 6.254944e-02 | 1.204 | 0 | 0 |
| SARS-CoV-2 targets PDZ proteins in cell-cell junction | R-HSA-9705677 | 6.348530e-02 | 1.197 | 0 | 0 |
| RUNX2 regulates genes involved in differentiation of myeloid cells | R-HSA-8941333 | 6.348530e-02 | 1.197 | 0 | 0 |
| Release of apoptotic factors from the mitochondria | R-HSA-111457 | 8.374343e-02 | 1.077 | 0 | 0 |
| Phosphorylation of Emi1 | R-HSA-176417 | 8.374343e-02 | 1.077 | 0 | 0 |
| ABC transporter disorders | R-HSA-5619084 | 6.910304e-02 | 1.161 | 0 | 0 |
| Golgi-to-ER retrograde transport | R-HSA-8856688 | 8.036087e-02 | 1.095 | 0 | 0 |
| FLT3 signaling through SRC family kinases | R-HSA-9706374 | 6.348530e-02 | 1.197 | 0 | 0 |
| Signaling by Erythropoietin | R-HSA-9006335 | 5.675640e-02 | 1.246 | 1 | 1 |
| Formation of Fibrin Clot (Clotting Cascade) | R-HSA-140877 | 8.103056e-02 | 1.091 | 0 | 0 |
| Regulation of CDH19 Expression and Function | R-HSA-9764302 | 8.374343e-02 | 1.077 | 0 | 0 |
| Anti-inflammatory response favouring Leishmania parasite infection | R-HSA-9662851 | 6.084556e-02 | 1.216 | 1 | 0 |
| Leishmania parasite growth and survival | R-HSA-9664433 | 6.084556e-02 | 1.216 | 1 | 0 |
| ESR-mediated signaling | R-HSA-8939211 | 6.434232e-02 | 1.192 | 0 | 0 |
| Sensory processing of sound | R-HSA-9659379 | 7.099409e-02 | 1.149 | 0 | 0 |
| Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZO1 and integrins in endothelial cells | R-HSA-9860927 | 7.784332e-02 | 1.109 | 0 | 0 |
| Extrinsic Pathway of Fibrin Clot Formation | R-HSA-140834 | 6.348530e-02 | 1.197 | 0 | 0 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | R-HSA-6814122 | 7.469719e-02 | 1.127 | 0 | 0 |
| G1/S-Specific Transcription | R-HSA-69205 | 8.103056e-02 | 1.091 | 0 | 0 |
| Regulation of TP53 Degradation | R-HSA-6804757 | 8.103056e-02 | 1.091 | 0 | 0 |
| TRAF6 mediated IRF7 activation | R-HSA-933541 | 8.425763e-02 | 1.074 | 0 | 0 |
| Regulation of PD-L1(CD274) Post-translational modification | R-HSA-9909615 | 8.486795e-02 | 1.071 | 0 | 0 |
| Regulation of TP53 Expression and Degradation | R-HSA-6806003 | 9.082640e-02 | 1.042 | 0 | 0 |
| Co-inhibition by PD-1 | R-HSA-389948 | 9.368928e-02 | 1.028 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in WNT signaling | R-HSA-8939256 | 9.370848e-02 | 1.028 | 0 | 0 |
| G2/M DNA replication checkpoint | R-HSA-69478 | 9.370848e-02 | 1.028 | 0 | 0 |
| E2F-enabled inhibition of pre-replication complex formation | R-HSA-113507 | 9.370848e-02 | 1.028 | 0 | 0 |
| Signaling by LTK in cancer | R-HSA-9842640 | 9.370848e-02 | 1.028 | 0 | 0 |
| Activation of NIMA Kinases NEK9, NEK6, NEK7 | R-HSA-2980767 | 9.370848e-02 | 1.028 | 0 | 0 |
| Defective factor VIII causes hemophilia A | R-HSA-9662001 | 9.370848e-02 | 1.028 | 0 | 0 |
| Transport of gamma-carboxylated protein precursors from the endoplasmic reticulum to the Golgi apparatus | R-HSA-159763 | 9.370848e-02 | 1.028 | 0 | 0 |
| Generation of second messenger molecules | R-HSA-202433 | 9.416570e-02 | 1.026 | 0 | 0 |
| Attenuation phase | R-HSA-3371568 | 9.416570e-02 | 1.026 | 0 | 0 |
| GPCR downstream signalling | R-HSA-388396 | 9.731881e-02 | 1.012 | 0 | 0 |
| M-decay: degradation of maternal mRNAs by maternally stored factors | R-HSA-9820841 | 9.754005e-02 | 1.011 | 0 | 0 |
| SPOP-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929491 | 9.754005e-02 | 1.011 | 0 | 0 |
| Translesion synthesis by Y family DNA polymerases bypasses lesions on DNA template | R-HSA-110313 | 9.754005e-02 | 1.011 | 0 | 0 |
| FLT3 Signaling | R-HSA-9607240 | 9.754005e-02 | 1.011 | 0 | 0 |
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | R-HSA-9705671 | 9.964337e-02 | 1.002 | 0 | 0 |
| RUNX3 regulates WNT signaling | R-HSA-8951430 | 1.035658e-01 | 0.985 | 0 | 0 |
| Binding of TCF/LEF:CTNNB1 to target gene promoters | R-HSA-4411364 | 1.035658e-01 | 0.985 | 0 | 0 |
| TRIF-mediated programmed cell death | R-HSA-2562578 | 1.035658e-01 | 0.985 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of myeloid cells | R-HSA-8939246 | 1.133165e-01 | 0.946 | 0 | 0 |
| Type I hemidesmosome assembly | R-HSA-446107 | 1.133165e-01 | 0.946 | 0 | 0 |
| Interleukin-21 signaling | R-HSA-9020958 | 1.229617e-01 | 0.910 | 0 | 0 |
| ALK mutants bind TKIs | R-HSA-9700645 | 1.229617e-01 | 0.910 | 0 | 0 |
| Defective factor IX causes hemophilia B | R-HSA-9668250 | 1.325026e-01 | 0.878 | 0 | 0 |
| Erythropoietin activates Phospholipase C gamma (PLCG) | R-HSA-9027277 | 1.325026e-01 | 0.878 | 1 | 1 |
| NF-kB activation through FADD/RIP-1 pathway mediated by caspase-8 and -10 | R-HSA-933543 | 1.419402e-01 | 0.848 | 0 | 0 |
| Sema4D mediated inhibition of cell attachment and migration | R-HSA-416550 | 1.512758e-01 | 0.820 | 0 | 0 |
| Signaling by GSK3beta mutants | R-HSA-5339716 | 1.512758e-01 | 0.820 | 0 | 0 |
| Signaling by CTNNB1 phospho-site mutants | R-HSA-4839743 | 1.605104e-01 | 0.794 | 0 | 0 |
| Scavenging by Class F Receptors | R-HSA-3000484 | 1.605104e-01 | 0.794 | 0 | 0 |
| CTNNB1 S33 mutants aren't phosphorylated | R-HSA-5358747 | 1.605104e-01 | 0.794 | 0 | 0 |
| CTNNB1 T41 mutants aren't phosphorylated | R-HSA-5358752 | 1.605104e-01 | 0.794 | 0 | 0 |
| CTNNB1 S37 mutants aren't phosphorylated | R-HSA-5358749 | 1.605104e-01 | 0.794 | 0 | 0 |
| CTNNB1 S45 mutants aren't phosphorylated | R-HSA-5358751 | 1.605104e-01 | 0.794 | 0 | 0 |
| RUNX1 and FOXP3 control the development of regulatory T lymphocytes (Tregs) | R-HSA-8877330 | 1.696451e-01 | 0.770 | 0 | 0 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | R-HSA-9661069 | 1.696451e-01 | 0.770 | 0 | 0 |
| ERBB2 Activates PTK6 Signaling | R-HSA-8847993 | 1.786809e-01 | 0.748 | 0 | 0 |
| TGF-beta receptor signaling in EMT (epithelial to mesenchymal transition) | R-HSA-2173791 | 1.876190e-01 | 0.727 | 0 | 0 |
| TRAF6-mediated induction of TAK1 complex within TLR4 complex | R-HSA-937072 | 1.876190e-01 | 0.727 | 0 | 0 |
| Beta-catenin phosphorylation cascade | R-HSA-196299 | 1.876190e-01 | 0.727 | 0 | 0 |
| ERBB2 Regulates Cell Motility | R-HSA-6785631 | 1.876190e-01 | 0.727 | 0 | 0 |
| GRB2:SOS provides linkage to MAPK signaling for Integrins | R-HSA-354194 | 1.964603e-01 | 0.707 | 0 | 0 |
| Defective CFTR causes cystic fibrosis | R-HSA-5678895 | 1.148981e-01 | 0.940 | 0 | 0 |
| Signaling by BRAF and RAF1 fusions | R-HSA-6802952 | 1.902742e-01 | 0.721 | 0 | 0 |
| RUNX1 regulates estrogen receptor mediated transcription | R-HSA-8931987 | 1.035658e-01 | 0.985 | 0 | 0 |
| Nonsense-Mediated Decay (NMD) | R-HSA-927802 | 1.552076e-01 | 0.809 | 0 | 0 |
| Activated NTRK3 signals through PI3K | R-HSA-9603381 | 1.035658e-01 | 0.985 | 0 | 0 |
| Regulation of CDH11 function | R-HSA-9762292 | 1.325026e-01 | 0.878 | 0 | 0 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | R-HSA-975957 | 1.552076e-01 | 0.809 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of keratinocytes | R-HSA-8939242 | 1.133165e-01 | 0.946 | 0 | 0 |
| SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | R-HSA-399955 | 1.964603e-01 | 0.707 | 0 | 0 |
| Platelet Aggregation (Plug Formation) | R-HSA-76009 | 1.148981e-01 | 0.940 | 0 | 0 |
| Regulation of TBK1, IKKε-mediated activation of IRF3, IRF7 upon TLR3 ligation | R-HSA-9828211 | 1.133165e-01 | 0.946 | 0 | 0 |
| Activated NTRK2 signals through CDK5 | R-HSA-9032845 | 1.035658e-01 | 0.985 | 0 | 0 |
| vRNP Assembly | R-HSA-192905 | 1.419402e-01 | 0.848 | 0 | 0 |
| Conjugation of benzoate with glycine | R-HSA-177135 | 1.419402e-01 | 0.848 | 0 | 0 |
| Constitutive Signaling by Overexpressed ERBB2 | R-HSA-9634285 | 1.605104e-01 | 0.794 | 0 | 0 |
| Downregulation of ERBB2:ERBB3 signaling | R-HSA-1358803 | 1.605104e-01 | 0.794 | 0 | 0 |
| Conjugation of salicylate with glycine | R-HSA-177128 | 1.605104e-01 | 0.794 | 0 | 0 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | R-HSA-9659787 | 1.696451e-01 | 0.770 | 0 | 0 |
| Phosphorylation of the APC/C | R-HSA-176412 | 1.964603e-01 | 0.707 | 0 | 0 |
| COPI-independent Golgi-to-ER retrograde traffic | R-HSA-6811436 | 1.516288e-01 | 0.819 | 0 | 0 |
| Role of phospholipids in phagocytosis | R-HSA-2029485 | 1.683267e-01 | 0.774 | 0 | 0 |
| PI3K/AKT activation | R-HSA-198203 | 1.325026e-01 | 0.878 | 0 | 0 |
| TICAM1-dependent activation of IRF3/IRF7 | R-HSA-9013973 | 1.512758e-01 | 0.820 | 0 | 0 |
| p38MAPK events | R-HSA-171007 | 1.876190e-01 | 0.727 | 0 | 0 |
| Deadenylation-dependent mRNA decay | R-HSA-429914 | 1.669045e-01 | 0.778 | 0 | 0 |
| Resolution of Sister Chromatid Cohesion | R-HSA-2500257 | 1.844765e-01 | 0.734 | 0 | 0 |
| Estrogen biosynthesis | R-HSA-193144 | 1.605104e-01 | 0.794 | 0 | 0 |
| Erythropoietin activates RAS | R-HSA-9027284 | 1.876190e-01 | 0.727 | 1 | 1 |
| G1/S Transition | R-HSA-69206 | 1.982354e-01 | 0.703 | 0 | 0 |
| NCAM signaling for neurite out-growth | R-HSA-375165 | 1.785291e-01 | 0.748 | 0 | 0 |
| Activation of SMO | R-HSA-5635838 | 1.964603e-01 | 0.707 | 0 | 0 |
| Dectin-2 family | R-HSA-5621480 | 1.592320e-01 | 0.798 | 1 | 1 |
| ABC-family proteins mediated transport | R-HSA-382556 | 1.227884e-01 | 0.911 | 0 | 0 |
| Diseases associated with surfactant metabolism | R-HSA-5687613 | 1.605104e-01 | 0.794 | 0 | 0 |
| Signaling by PDGFRA extracellular domain mutants | R-HSA-9673770 | 1.876190e-01 | 0.727 | 0 | 0 |
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | R-HSA-9673767 | 1.876190e-01 | 0.727 | 0 | 0 |
| Regulation of APC/C activators between G1/S and early anaphase | R-HSA-176408 | 1.785291e-01 | 0.748 | 0 | 0 |
| Signaling by the B Cell Receptor (BCR) | R-HSA-983705 | 1.283339e-01 | 0.892 | 1 | 0 |
| Netrin mediated repulsion signals | R-HSA-418886 | 1.035658e-01 | 0.985 | 0 | 0 |
| MASTL Facilitates Mitotic Progression | R-HSA-2465910 | 1.229617e-01 | 0.910 | 0 | 0 |
| MAPK3 (ERK1) activation | R-HSA-110056 | 1.325026e-01 | 0.878 | 0 | 0 |
| Cholesterol biosynthesis via desmosterol | R-HSA-6807047 | 1.419402e-01 | 0.848 | 0 | 0 |
| Synthesis of diphthamide-EEF2 | R-HSA-5358493 | 1.512758e-01 | 0.820 | 0 | 0 |
| RUNX3 regulates p14-ARF | R-HSA-8951936 | 1.605104e-01 | 0.794 | 0 | 0 |
| Advanced glycosylation endproduct receptor signaling | R-HSA-879415 | 1.605104e-01 | 0.794 | 0 | 0 |
| Platelet Adhesion to exposed collagen | R-HSA-75892 | 1.696451e-01 | 0.770 | 1 | 1 |
| Formation of axial mesoderm | R-HSA-9796292 | 1.696451e-01 | 0.770 | 0 | 0 |
| Protein lipoylation | R-HSA-9857492 | 1.876190e-01 | 0.727 | 0 | 0 |
| HSF1-dependent transactivation | R-HSA-3371571 | 1.366576e-01 | 0.864 | 0 | 0 |
| GP1b-IX-V activation signalling | R-HSA-430116 | 1.229617e-01 | 0.910 | 0 | 0 |
| Kinesins | R-HSA-983189 | 1.707648e-01 | 0.768 | 0 | 0 |
| Downregulation of ERBB4 signaling | R-HSA-1253288 | 1.133165e-01 | 0.946 | 0 | 0 |
| Regulation of commissural axon pathfinding by SLIT and ROBO | R-HSA-428542 | 1.229617e-01 | 0.910 | 0 | 0 |
| Synthesis of PIPs at the ER membrane | R-HSA-1483248 | 1.419402e-01 | 0.848 | 0 | 0 |
| Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | R-HSA-75035 | 1.696451e-01 | 0.770 | 0 | 0 |
| IRAK2 mediated activation of TAK1 complex upon TLR7/8 or 9 stimulation | R-HSA-975163 | 1.786809e-01 | 0.748 | 0 | 0 |
| Cargo recognition for clathrin-mediated endocytosis | R-HSA-8856825 | 1.324811e-01 | 0.878 | 0 | 0 |
| RSV-host interactions | R-HSA-9833110 | 1.349452e-01 | 0.870 | 0 | 0 |
| Cellular response to heat stress | R-HSA-3371556 | 1.844765e-01 | 0.734 | 0 | 0 |
| Josephin domain DUBs | R-HSA-5689877 | 1.325026e-01 | 0.878 | 0 | 0 |
| Golgi Cisternae Pericentriolar Stack Reorganization | R-HSA-162658 | 1.696451e-01 | 0.770 | 0 | 0 |
| Cilium Assembly | R-HSA-5617833 | 1.965153e-01 | 0.707 | 0 | 0 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | R-HSA-198933 | 1.387998e-01 | 0.858 | 0 | 0 |
| Antiviral mechanism by IFN-stimulated genes | R-HSA-1169410 | 1.208606e-01 | 0.918 | 0 | 0 |
| SARS-CoV-2-host interactions | R-HSA-9705683 | 1.371620e-01 | 0.863 | 0 | 0 |
| Transcriptional regulation of granulopoiesis | R-HSA-9616222 | 1.785291e-01 | 0.748 | 0 | 0 |
| Sensory processing of sound by outer hair cells of the cochlea | R-HSA-9662361 | 1.554213e-01 | 0.808 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | R-HSA-6804116 | 1.964603e-01 | 0.707 | 0 | 0 |
| DNA Damage Bypass | R-HSA-73893 | 1.293039e-01 | 0.888 | 0 | 0 |
| Removal of aminoterminal propeptides from gamma-carboxylated proteins | R-HSA-159782 | 1.035658e-01 | 0.985 | 0 | 0 |
| Gamma-carboxylation of protein precursors | R-HSA-159740 | 1.512758e-01 | 0.820 | 0 | 0 |
| Gamma-carboxylation, transport, and amino-terminal cleavage of proteins | R-HSA-159854 | 1.605104e-01 | 0.794 | 0 | 0 |
| Caspase activation via Death Receptors in the presence of ligand | R-HSA-140534 | 1.964603e-01 | 0.707 | 0 | 0 |
| Regulation of PD-L1(CD274) expression | R-HSA-9909648 | 1.579835e-01 | 0.801 | 0 | 0 |
| Interleukin-2 signaling | R-HSA-9020558 | 1.419402e-01 | 0.848 | 0 | 0 |
| Apoptotic cleavage of cell adhesion proteins | R-HSA-351906 | 1.133165e-01 | 0.946 | 0 | 0 |
| Signaling by LTK | R-HSA-9842663 | 1.605104e-01 | 0.794 | 0 | 0 |
| Attachment and Entry | R-HSA-9678110 | 1.964603e-01 | 0.707 | 0 | 0 |
| Spry regulation of FGF signaling | R-HSA-1295596 | 1.876190e-01 | 0.727 | 0 | 0 |
| Negative regulation of FLT3 | R-HSA-9706369 | 1.964603e-01 | 0.707 | 0 | 0 |
| Atorvastatin ADME | R-HSA-9754706 | 1.964603e-01 | 0.707 | 0 | 0 |
| Cellular responses to stimuli | R-HSA-8953897 | 1.383114e-01 | 0.859 | 0 | 0 |
| MITF-M-regulated melanocyte development | R-HSA-9730414 | 1.136752e-01 | 0.944 | 0 | 0 |
| TP53 Regulates Transcription of Cell Cycle Genes | R-HSA-6791312 | 1.592320e-01 | 0.798 | 0 | 0 |
| Differentiation of naive CD+ T cells to T helper 1 cells (Th1 cells) | R-HSA-9942503 | 1.964603e-01 | 0.707 | 0 | 0 |
| Differentiation of T cells | R-HSA-9945266 | 1.964603e-01 | 0.707 | 0 | 0 |
| Synthesis of PIPs at the plasma membrane | R-HSA-1660499 | 1.785291e-01 | 0.748 | 0 | 0 |
| FOXO-mediated transcription of oxidative stress, metabolic and neuronal genes | R-HSA-9615017 | 1.009483e-01 | 0.996 | 0 | 0 |
| Synthesis of PC | R-HSA-1483191 | 1.220481e-01 | 0.913 | 0 | 0 |
| Infectious disease | R-HSA-5663205 | 1.226325e-01 | 0.911 | 1 | 0 |
| Signaling by GPCR | R-HSA-372790 | 1.658983e-01 | 0.780 | 0 | 0 |
| SARS-CoV Infections | R-HSA-9679506 | 1.018624e-01 | 0.992 | 0 | 0 |
| Viral Infection Pathways | R-HSA-9824446 | 1.254596e-01 | 0.901 | 0 | 0 |
| PI Metabolism | R-HSA-1483255 | 1.276014e-01 | 0.894 | 0 | 0 |
| Interleukin-4 and Interleukin-13 signaling | R-HSA-6785807 | 2.009667e-01 | 0.697 | 0 | 0 |
| Drug ADME | R-HSA-9748784 | 1.212739e-01 | 0.916 | 0 | 0 |
| MHC class II antigen presentation | R-HSA-2132295 | 1.899493e-01 | 0.721 | 0 | 0 |
| Nuclear events stimulated by ALK signaling in cancer | R-HSA-9725371 | 1.256633e-01 | 0.901 | 0 | 0 |
| Uptake and actions of bacterial toxins | R-HSA-5339562 | 1.403688e-01 | 0.853 | 0 | 0 |
| Sensory processing of sound by inner hair cells of the cochlea | R-HSA-9662360 | 2.021201e-01 | 0.694 | 0 | 0 |
| Regulated Necrosis | R-HSA-5218859 | 2.021201e-01 | 0.694 | 0 | 0 |
| Defects of contact activation system (CAS) and kallikrein/kinin system (KKS) | R-HSA-9651496 | 2.052059e-01 | 0.688 | 0 | 0 |
| Fibronectin matrix formation | R-HSA-1566977 | 2.052059e-01 | 0.688 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | R-HSA-6804114 | 2.052059e-01 | 0.688 | 0 | 0 |
| Developmental Lineage of Pancreatic Ductal Cells | R-HSA-9925563 | 2.060878e-01 | 0.686 | 0 | 0 |
| Signaling by NTRK1 (TRKA) | R-HSA-187037 | 2.066077e-01 | 0.685 | 0 | 0 |
| Constitutive Signaling by EGFRvIII | R-HSA-5637810 | 2.138569e-01 | 0.670 | 0 | 0 |
| Signaling by EGFRvIII in Cancer | R-HSA-5637812 | 2.138569e-01 | 0.670 | 0 | 0 |
| p130Cas linkage to MAPK signaling for integrins | R-HSA-372708 | 2.138569e-01 | 0.670 | 0 | 0 |
| PI3K events in ERBB2 signaling | R-HSA-1963642 | 2.138569e-01 | 0.670 | 0 | 0 |
| Modulation of host responses by IFN-stimulated genes | R-HSA-9909505 | 2.138569e-01 | 0.670 | 0 | 0 |
| APC/C-mediated degradation of cell cycle proteins | R-HSA-174143 | 2.140481e-01 | 0.669 | 0 | 0 |
| Regulation of mitotic cell cycle | R-HSA-453276 | 2.140481e-01 | 0.669 | 0 | 0 |
| SARS-CoV-2 Infection | R-HSA-9694516 | 2.182708e-01 | 0.661 | 0 | 0 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | R-HSA-6811442 | 2.190654e-01 | 0.659 | 0 | 0 |
| Circadian clock | R-HSA-9909396 | 2.207347e-01 | 0.656 | 0 | 0 |
| Aspirin ADME | R-HSA-9749641 | 2.220370e-01 | 0.654 | 0 | 0 |
| Platelet sensitization by LDL | R-HSA-432142 | 2.224143e-01 | 0.653 | 0 | 0 |
| ZBP1(DAI) mediated induction of type I IFNs | R-HSA-1606322 | 2.224143e-01 | 0.653 | 0 | 0 |
| Depolymerization of the Nuclear Lamina | R-HSA-4419969 | 2.224143e-01 | 0.653 | 0 | 0 |
| Signaling by ERBB2 ECD mutants | R-HSA-9665348 | 2.224143e-01 | 0.653 | 0 | 0 |
| Biosynthesis of Lipoxins (LX) | R-HSA-2142700 | 2.224143e-01 | 0.653 | 0 | 0 |
| Apoptotic factor-mediated response | R-HSA-111471 | 2.224143e-01 | 0.653 | 0 | 0 |
| Tie2 Signaling | R-HSA-210993 | 2.224143e-01 | 0.653 | 0 | 0 |
| Signaling by ERBB4 | R-HSA-1236394 | 2.260407e-01 | 0.646 | 0 | 0 |
| IKK complex recruitment mediated by RIP1 | R-HSA-937041 | 2.308791e-01 | 0.637 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Cyclin B | R-HSA-174048 | 2.308791e-01 | 0.637 | 0 | 0 |
| Germ layer formation at gastrulation | R-HSA-9754189 | 2.308791e-01 | 0.637 | 0 | 0 |
| Specification of the neural plate border | R-HSA-9834899 | 2.308791e-01 | 0.637 | 0 | 0 |
| Conjugation of carboxylic acids | R-HSA-159424 | 2.308791e-01 | 0.637 | 0 | 0 |
| Amino Acid conjugation | R-HSA-156587 | 2.308791e-01 | 0.637 | 0 | 0 |
| Diseases of hemostasis | R-HSA-9671793 | 2.308791e-01 | 0.637 | 0 | 0 |
| Translesion Synthesis by POLH | R-HSA-110320 | 2.308791e-01 | 0.637 | 0 | 0 |
| E2F mediated regulation of DNA replication | R-HSA-113510 | 2.308791e-01 | 0.637 | 0 | 0 |
| The NLRP3 inflammasome | R-HSA-844456 | 2.308791e-01 | 0.637 | 0 | 0 |
| Mechanical load activates signaling by PIEZO1 and integrins in osteocytes | R-HSA-9856532 | 2.308791e-01 | 0.637 | 0 | 0 |
| Estrogen-dependent gene expression | R-HSA-9018519 | 2.350518e-01 | 0.629 | 0 | 0 |
| Formation of ATP by chemiosmotic coupling | R-HSA-163210 | 2.392522e-01 | 0.621 | 0 | 0 |
| Sema4D induced cell migration and growth-cone collapse | R-HSA-416572 | 2.392522e-01 | 0.621 | 0 | 0 |
| Common Pathway of Fibrin Clot Formation | R-HSA-140875 | 2.392522e-01 | 0.621 | 0 | 0 |
| Creatine metabolism | R-HSA-71288 | 2.392522e-01 | 0.621 | 0 | 0 |
| Formation of definitive endoderm | R-HSA-9823730 | 2.392522e-01 | 0.621 | 0 | 0 |
| Protein hydroxylation | R-HSA-9629569 | 2.392522e-01 | 0.621 | 0 | 0 |
| Signaling by Nuclear Receptors | R-HSA-9006931 | 2.429685e-01 | 0.614 | 0 | 0 |
| PTEN Regulation | R-HSA-6807070 | 2.437209e-01 | 0.613 | 0 | 0 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | R-HSA-5637815 | 2.475346e-01 | 0.606 | 0 | 0 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | R-HSA-1236382 | 2.475346e-01 | 0.606 | 0 | 0 |
| MyD88 deficiency (TLR2/4) | R-HSA-5602498 | 2.475346e-01 | 0.606 | 0 | 0 |
| TNFR1-induced proapoptotic signaling | R-HSA-5357786 | 2.475346e-01 | 0.606 | 0 | 0 |
| Intrinsic Pathway of Fibrin Clot Formation | R-HSA-140837 | 2.475346e-01 | 0.606 | 0 | 0 |
| Signalling to RAS | R-HSA-167044 | 2.475346e-01 | 0.606 | 0 | 0 |
| Signaling by FGFR2 | R-HSA-5654738 | 2.501552e-01 | 0.602 | 0 | 0 |
| PKR-mediated signaling | R-HSA-9833482 | 2.501552e-01 | 0.602 | 0 | 0 |
| IRAK4 deficiency (TLR2/4) | R-HSA-5603041 | 2.557274e-01 | 0.592 | 0 | 0 |
| Signaling by NTRK3 (TRKC) | R-HSA-9034015 | 2.557274e-01 | 0.592 | 0 | 0 |
| Signaling by PDGFR in disease | R-HSA-9671555 | 2.557274e-01 | 0.592 | 0 | 0 |
| Initiation of Nuclear Envelope (NE) Reformation | R-HSA-2995383 | 2.557274e-01 | 0.592 | 0 | 0 |
| Attachment and Entry | R-HSA-9694614 | 2.557274e-01 | 0.592 | 0 | 0 |
| Clathrin-mediated endocytosis | R-HSA-8856828 | 2.582806e-01 | 0.588 | 0 | 0 |
| Phospholipid metabolism | R-HSA-1483257 | 2.627657e-01 | 0.580 | 0 | 0 |
| FGFR2 alternative splicing | R-HSA-6803529 | 2.638315e-01 | 0.579 | 0 | 0 |
| Cholesterol biosynthesis via lathosterol | R-HSA-6807062 | 2.638315e-01 | 0.579 | 0 | 0 |
| RAF-independent MAPK1/3 activation | R-HSA-112409 | 2.638315e-01 | 0.579 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | R-HSA-8939236 | 2.662792e-01 | 0.575 | 0 | 0 |
| Oncogenic MAPK signaling | R-HSA-6802957 | 2.703114e-01 | 0.568 | 0 | 0 |
| Meiosis | R-HSA-1500620 | 2.703114e-01 | 0.568 | 0 | 0 |
| Formation of the ureteric bud | R-HSA-9830674 | 2.718479e-01 | 0.566 | 0 | 0 |
| Toll Like Receptor 4 (TLR4) Cascade | R-HSA-166016 | 2.729553e-01 | 0.564 | 0 | 0 |
| Amplification of signal from the kinetochores | R-HSA-141424 | 2.743432e-01 | 0.562 | 0 | 0 |
| Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal | R-HSA-141444 | 2.743432e-01 | 0.562 | 0 | 0 |
| Gamma carboxylation, hypusinylation, hydroxylation, and arylsulfatase activation | R-HSA-163841 | 2.783740e-01 | 0.555 | 0 | 0 |
| M Phase | R-HSA-68886 | 2.795806e-01 | 0.553 | 0 | 0 |
| Translocation of ZAP-70 to Immunological synapse | R-HSA-202430 | 2.797775e-01 | 0.553 | 0 | 0 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models | R-HSA-8862803 | 2.797775e-01 | 0.553 | 0 | 0 |
| Neurodegenerative Diseases | R-HSA-8863678 | 2.797775e-01 | 0.553 | 0 | 0 |
| TRAF6 mediated NF-kB activation | R-HSA-933542 | 2.797775e-01 | 0.553 | 0 | 0 |
| ADP signalling through P2Y purinoceptor 1 | R-HSA-418592 | 2.797775e-01 | 0.553 | 0 | 0 |
| CD209 (DC-SIGN) signaling | R-HSA-5621575 | 2.797775e-01 | 0.553 | 1 | 1 |
| KEAP1-NFE2L2 pathway | R-HSA-9755511 | 2.818040e-01 | 0.550 | 0 | 0 |
| Chaperonin-mediated protein folding | R-HSA-390466 | 2.824035e-01 | 0.549 | 0 | 0 |
| Developmental Cell Lineages of the Exocrine Pancreas | R-HSA-9820448 | 2.847596e-01 | 0.546 | 0 | 0 |
| Sema4D in semaphorin signaling | R-HSA-400685 | 2.876211e-01 | 0.541 | 0 | 0 |
| Long-term potentiation | R-HSA-9620244 | 2.876211e-01 | 0.541 | 0 | 0 |
| PIWI-interacting RNA (piRNA) biogenesis | R-HSA-5601884 | 2.876211e-01 | 0.541 | 0 | 0 |
| Downstream TCR signaling | R-HSA-202424 | 2.944792e-01 | 0.531 | 0 | 0 |
| Signaling by EGFR in Cancer | R-HSA-1643713 | 2.953799e-01 | 0.530 | 0 | 0 |
| MET activates PTK2 signaling | R-HSA-8874081 | 2.953799e-01 | 0.530 | 0 | 0 |
| Synthesis of PIPs at the Golgi membrane | R-HSA-1660514 | 2.953799e-01 | 0.530 | 0 | 0 |
| Caspase activation via extrinsic apoptotic signalling pathway | R-HSA-5357769 | 2.953799e-01 | 0.530 | 0 | 0 |
| Defective Intrinsic Pathway for Apoptosis | R-HSA-9734009 | 3.030546e-01 | 0.518 | 0 | 0 |
| Cristae formation | R-HSA-8949613 | 3.030546e-01 | 0.518 | 0 | 0 |
| Disassembly of the destruction complex and recruitment of AXIN to the membrane | R-HSA-4641262 | 3.030546e-01 | 0.518 | 0 | 0 |
| Protein folding | R-HSA-391251 | 3.065271e-01 | 0.514 | 0 | 0 |
| Membrane Trafficking | R-HSA-199991 | 3.103710e-01 | 0.508 | 0 | 0 |
| PINK1-PRKN Mediated Mitophagy | R-HSA-5205685 | 3.106462e-01 | 0.508 | 0 | 0 |
| Telomere Extension By Telomerase | R-HSA-171319 | 3.106462e-01 | 0.508 | 0 | 0 |
| Inflammasomes | R-HSA-622312 | 3.106462e-01 | 0.508 | 0 | 0 |
| Negative regulation of FGFR3 signaling | R-HSA-5654732 | 3.106462e-01 | 0.508 | 0 | 0 |
| Pyroptosis | R-HSA-5620971 | 3.106462e-01 | 0.508 | 0 | 0 |
| Organelle biogenesis and maintenance | R-HSA-1852241 | 3.152900e-01 | 0.501 | 0 | 0 |
| Late endosomal microautophagy | R-HSA-9615710 | 3.181556e-01 | 0.497 | 0 | 0 |
| Regulation of CDH11 Expression and Function | R-HSA-9759475 | 3.181556e-01 | 0.497 | 0 | 0 |
| Termination of translesion DNA synthesis | R-HSA-5656169 | 3.181556e-01 | 0.497 | 0 | 0 |
| DARPP-32 events | R-HSA-180024 | 3.181556e-01 | 0.497 | 0 | 0 |
| Negative regulation of FGFR4 signaling | R-HSA-5654733 | 3.181556e-01 | 0.497 | 0 | 0 |
| Ribosome Quality Control (RQC) complex extracts and degrades nascent peptide | R-HSA-9954709 | 3.225291e-01 | 0.491 | 0 | 0 |
| SHC1 events in ERBB2 signaling | R-HSA-1250196 | 3.255836e-01 | 0.487 | 0 | 0 |
| Activation of the pre-replicative complex | R-HSA-68962 | 3.255836e-01 | 0.487 | 0 | 0 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | R-HSA-9687139 | 3.255836e-01 | 0.487 | 0 | 0 |
| Thrombin signalling through proteinase activated receptors (PARs) | R-HSA-456926 | 3.255836e-01 | 0.487 | 0 | 0 |
| Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation | R-HSA-1474151 | 3.255836e-01 | 0.487 | 0 | 0 |
| Interleukin-37 signaling | R-HSA-9008059 | 3.255836e-01 | 0.487 | 0 | 0 |
| Role of LAT2/NTAL/LAB on calcium mobilization | R-HSA-2730905 | 3.265162e-01 | 0.486 | 1 | 1 |
| COPI-dependent Golgi-to-ER retrograde traffic | R-HSA-6811434 | 3.265162e-01 | 0.486 | 0 | 0 |
| CLEC7A (Dectin-1) signaling | R-HSA-5607764 | 3.265162e-01 | 0.486 | 0 | 0 |
| EGFR downregulation | R-HSA-182971 | 3.329311e-01 | 0.478 | 0 | 0 |
| Evasion by RSV of host interferon responses | R-HSA-9833109 | 3.329311e-01 | 0.478 | 0 | 0 |
| Cargo concentration in the ER | R-HSA-5694530 | 3.329311e-01 | 0.478 | 0 | 0 |
| Respiratory syncytial virus (RSV) attachment and entry | R-HSA-9820960 | 3.329311e-01 | 0.478 | 0 | 0 |
| Disorders of transmembrane transporters | R-HSA-5619115 | 3.342925e-01 | 0.476 | 0 | 0 |
| Signaling by FGFR | R-HSA-190236 | 3.344715e-01 | 0.476 | 0 | 0 |
| FOXO-mediated transcription | R-HSA-9614085 | 3.384392e-01 | 0.471 | 0 | 0 |
| Developmental Lineage of Multipotent Pancreatic Progenitor Cells | R-HSA-9937080 | 3.401991e-01 | 0.468 | 0 | 0 |
| Signaling by WNT in cancer | R-HSA-4791275 | 3.401991e-01 | 0.468 | 0 | 0 |
| Diseases of mitotic cell cycle | R-HSA-9675126 | 3.401991e-01 | 0.468 | 0 | 0 |
| Mitotic Spindle Checkpoint | R-HSA-69618 | 3.423999e-01 | 0.465 | 0 | 0 |
| C-type lectin receptors (CLRs) | R-HSA-5621481 | 3.441758e-01 | 0.463 | 1 | 0 |
| Regulation of Expression and Function of Type II Classical Cadherins | R-HSA-9764260 | 3.473883e-01 | 0.459 | 0 | 0 |
| Activation of ATR in response to replication stress | R-HSA-176187 | 3.473883e-01 | 0.459 | 0 | 0 |
| HDR through Single Strand Annealing (SSA) | R-HSA-5685938 | 3.473883e-01 | 0.459 | 0 | 0 |
| Regulation of necroptotic cell death | R-HSA-5675482 | 3.473883e-01 | 0.459 | 0 | 0 |
| Synthesis of IP3 and IP4 in the cytosol | R-HSA-1855204 | 3.473883e-01 | 0.459 | 0 | 0 |
| Cardiogenesis | R-HSA-9733709 | 3.473883e-01 | 0.459 | 0 | 0 |
| Negative regulation of FGFR1 signaling | R-HSA-5654726 | 3.473883e-01 | 0.459 | 0 | 0 |
| Deubiquitination | R-HSA-5688426 | 3.540396e-01 | 0.451 | 0 | 0 |
| Heme degradation | R-HSA-189483 | 3.544996e-01 | 0.450 | 0 | 0 |
| Opioid Signalling | R-HSA-111885 | 3.581652e-01 | 0.446 | 0 | 0 |
| Generic Transcription Pathway | R-HSA-212436 | 3.586278e-01 | 0.445 | 0 | 0 |
| Cell Cycle Checkpoints | R-HSA-69620 | 3.614493e-01 | 0.442 | 0 | 0 |
| Regulation of TLR by endogenous ligand | R-HSA-5686938 | 3.615339e-01 | 0.442 | 0 | 0 |
| eNOS activation | R-HSA-203615 | 3.615339e-01 | 0.442 | 0 | 0 |
| SARS-CoV-1 modulates host translation machinery | R-HSA-9735869 | 3.615339e-01 | 0.442 | 0 | 0 |
| RAF activation | R-HSA-5673000 | 3.615339e-01 | 0.442 | 0 | 0 |
| Negative regulation of FGFR2 signaling | R-HSA-5654727 | 3.615339e-01 | 0.442 | 0 | 0 |
| Signal amplification | R-HSA-392518 | 3.615339e-01 | 0.442 | 0 | 0 |
| Nuclear Pore Complex (NPC) Disassembly | R-HSA-3301854 | 3.684919e-01 | 0.434 | 0 | 0 |
| Signalling to ERKs | R-HSA-187687 | 3.684919e-01 | 0.434 | 0 | 0 |
| Calmodulin induced events | R-HSA-111933 | 3.753746e-01 | 0.426 | 0 | 0 |
| CaM pathway | R-HSA-111997 | 3.753746e-01 | 0.426 | 0 | 0 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | R-HSA-72706 | 3.776770e-01 | 0.423 | 0 | 0 |
| L13a-mediated translational silencing of Ceruloplasmin expression | R-HSA-156827 | 3.776770e-01 | 0.423 | 0 | 0 |
| TCF dependent signaling in response to WNT | R-HSA-201681 | 3.797229e-01 | 0.421 | 0 | 0 |
| EML4 and NUDC in mitotic spindle formation | R-HSA-9648025 | 3.815506e-01 | 0.418 | 0 | 0 |
| Deactivation of the beta-catenin transactivating complex | R-HSA-3769402 | 3.821826e-01 | 0.418 | 0 | 0 |
| Signaling by high-kinase activity BRAF mutants | R-HSA-6802948 | 3.821826e-01 | 0.418 | 0 | 0 |
| SLC-mediated transport of organic cations | R-HSA-549127 | 3.821826e-01 | 0.418 | 0 | 0 |
| MyD88-independent TLR4 cascade | R-HSA-166166 | 3.854141e-01 | 0.414 | 0 | 0 |
| TRIF (TICAM1)-mediated TLR4 signaling | R-HSA-937061 | 3.854141e-01 | 0.414 | 0 | 0 |
| Cellular response to chemical stress | R-HSA-9711123 | 3.861213e-01 | 0.413 | 0 | 0 |
| Metabolism of nitric oxide: NOS3 activation and regulation | R-HSA-202131 | 3.889169e-01 | 0.410 | 0 | 0 |
| MET promotes cell motility | R-HSA-8875878 | 3.889169e-01 | 0.410 | 0 | 0 |
| RIPK1-mediated regulated necrosis | R-HSA-5213460 | 3.889169e-01 | 0.410 | 0 | 0 |
| Synthesis, secretion, and inactivation of Glucagon-like Peptide-1 (GLP-1) | R-HSA-381771 | 3.955782e-01 | 0.403 | 0 | 0 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | R-HSA-5693567 | 4.007621e-01 | 0.397 | 0 | 0 |
| Regulation of RUNX3 expression and activity | R-HSA-8941858 | 4.021672e-01 | 0.396 | 0 | 0 |
| Diseases of Immune System | R-HSA-5260271 | 4.021672e-01 | 0.396 | 0 | 0 |
| Diseases associated with the TLR signaling cascade | R-HSA-5602358 | 4.021672e-01 | 0.396 | 0 | 0 |
| Nuclear signaling by ERBB4 | R-HSA-1251985 | 4.021672e-01 | 0.396 | 0 | 0 |
| Toll-like Receptor Cascades | R-HSA-168898 | 4.032068e-01 | 0.394 | 0 | 0 |
| Hh mutants are degraded by ERAD | R-HSA-5362768 | 4.086849e-01 | 0.389 | 0 | 0 |
| Transcriptional Regulation by VENTX | R-HSA-8853884 | 4.086849e-01 | 0.389 | 0 | 0 |
| RNA Polymerase II Transcription | R-HSA-73857 | 4.146643e-01 | 0.382 | 0 | 0 |
| Signaling by RAF1 mutants | R-HSA-9656223 | 4.151319e-01 | 0.382 | 0 | 0 |
| MAP2K and MAPK activation | R-HSA-5674135 | 4.151319e-01 | 0.382 | 0 | 0 |
| SLC-mediated transport of neurotransmitters | R-HSA-442660 | 4.151319e-01 | 0.382 | 0 | 0 |
| Eukaryotic Translation Initiation | R-HSA-72613 | 4.159298e-01 | 0.381 | 0 | 0 |
| Cap-dependent Translation Initiation | R-HSA-72737 | 4.159298e-01 | 0.381 | 0 | 0 |
| Vesicle-mediated transport | R-HSA-5653656 | 4.207686e-01 | 0.376 | 0 | 0 |
| Ca-dependent events | R-HSA-111996 | 4.215089e-01 | 0.375 | 0 | 0 |
| Incretin synthesis, secretion, and inactivation | R-HSA-400508 | 4.215089e-01 | 0.375 | 0 | 0 |
| Homology Directed Repair | R-HSA-5693538 | 4.234421e-01 | 0.373 | 0 | 0 |
| Hh mutants abrogate ligand secretion | R-HSA-5387390 | 4.278169e-01 | 0.369 | 0 | 0 |
| Signaling by FGFR4 | R-HSA-5654743 | 4.278169e-01 | 0.369 | 0 | 0 |
| SCF(Skp2)-mediated degradation of p27/p21 | R-HSA-187577 | 4.340564e-01 | 0.362 | 0 | 0 |
| Surfactant metabolism | R-HSA-5683826 | 4.340564e-01 | 0.362 | 0 | 0 |
| Synthesis of Leukotrienes (LT) and Eoxins (EX) | R-HSA-2142691 | 4.340564e-01 | 0.362 | 0 | 0 |
| RMTs methylate histone arginines | R-HSA-3214858 | 4.340564e-01 | 0.362 | 0 | 0 |
| Somitogenesis | R-HSA-9824272 | 4.402283e-01 | 0.356 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in pigmentation | R-HSA-9824585 | 4.402283e-01 | 0.356 | 0 | 0 |
| DAG and IP3 signaling | R-HSA-1489509 | 4.402283e-01 | 0.356 | 0 | 0 |
| Signaling by FGFR3 | R-HSA-5654741 | 4.402283e-01 | 0.356 | 0 | 0 |
| Maternal to zygotic transition (MZT) | R-HSA-9816359 | 4.420024e-01 | 0.355 | 0 | 0 |
| Host Interactions of HIV factors | R-HSA-162909 | 4.456753e-01 | 0.351 | 0 | 0 |
| Signaling downstream of RAS mutants | R-HSA-9649948 | 4.463333e-01 | 0.350 | 0 | 0 |
| Signaling by moderate kinase activity BRAF mutants | R-HSA-6802946 | 4.463333e-01 | 0.350 | 0 | 0 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF | R-HSA-6802955 | 4.463333e-01 | 0.350 | 0 | 0 |
| Signaling by RAS mutants | R-HSA-6802949 | 4.463333e-01 | 0.350 | 0 | 0 |
| Condensation of Prophase Chromosomes | R-HSA-2299718 | 4.463333e-01 | 0.350 | 0 | 0 |
| Cell recruitment (pro-inflammatory response) | R-HSA-9664424 | 4.463333e-01 | 0.350 | 0 | 0 |
| Purinergic signaling in leishmaniasis infection | R-HSA-9660826 | 4.463333e-01 | 0.350 | 0 | 0 |
| Regulation of TNFR1 signaling | R-HSA-5357905 | 4.463333e-01 | 0.350 | 0 | 0 |
| Recycling pathway of L1 | R-HSA-437239 | 4.523721e-01 | 0.345 | 0 | 0 |
| Interferon Signaling | R-HSA-913531 | 4.528078e-01 | 0.344 | 0 | 0 |
| Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | R-HSA-9851695 | 4.529809e-01 | 0.344 | 0 | 0 |
| MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis | R-HSA-9841922 | 4.529809e-01 | 0.344 | 0 | 0 |
| Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | R-HSA-9818564 | 4.529809e-01 | 0.344 | 0 | 0 |
| GPER1 signaling | R-HSA-9634597 | 4.583453e-01 | 0.339 | 0 | 0 |
| NGF-stimulated transcription | R-HSA-9031628 | 4.583453e-01 | 0.339 | 0 | 0 |
| G2/M Checkpoints | R-HSA-69481 | 4.602319e-01 | 0.337 | 0 | 0 |
| Metabolism of RNA | R-HSA-8953854 | 4.606165e-01 | 0.337 | 0 | 0 |
| Gap junction trafficking and regulation | R-HSA-157858 | 4.642538e-01 | 0.333 | 0 | 0 |
| p53-Dependent G1 DNA Damage Response | R-HSA-69563 | 4.642538e-01 | 0.333 | 0 | 0 |
| p53-Dependent G1/S DNA damage checkpoint | R-HSA-69580 | 4.642538e-01 | 0.333 | 0 | 0 |
| N-glycan trimming in the ER and Calnexin/Calreticulin cycle | R-HSA-532668 | 4.642538e-01 | 0.333 | 0 | 0 |
| Chemokine receptors bind chemokines | R-HSA-380108 | 4.642538e-01 | 0.333 | 0 | 0 |
| Regulation of RAS by GAPs | R-HSA-5658442 | 4.700982e-01 | 0.328 | 0 | 0 |
| PI3K Cascade | R-HSA-109704 | 4.700982e-01 | 0.328 | 0 | 0 |
| Reproduction | R-HSA-1474165 | 4.745655e-01 | 0.324 | 0 | 0 |
| Hedgehog ligand biogenesis | R-HSA-5358346 | 4.758792e-01 | 0.323 | 0 | 0 |
| Meiotic recombination | R-HSA-912446 | 4.758792e-01 | 0.323 | 0 | 0 |
| Mitotic Anaphase | R-HSA-68882 | 4.774639e-01 | 0.321 | 0 | 0 |
| Mitotic Metaphase and Anaphase | R-HSA-2555396 | 4.802396e-01 | 0.319 | 0 | 0 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | R-HSA-174184 | 4.815974e-01 | 0.317 | 0 | 0 |
| mRNA 3'-end processing | R-HSA-72187 | 4.815974e-01 | 0.317 | 0 | 0 |
| AMPK-induced ERAD and lysosome mediated degradation of PD-L1(CD274) | R-HSA-9931269 | 4.815974e-01 | 0.317 | 0 | 0 |
| Orc1 removal from chromatin | R-HSA-68949 | 4.815974e-01 | 0.317 | 0 | 0 |
| E3 ubiquitin ligases ubiquitinate target proteins | R-HSA-8866654 | 4.815974e-01 | 0.317 | 0 | 0 |
| Neurexins and neuroligins | R-HSA-6794361 | 4.815974e-01 | 0.317 | 0 | 0 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | R-HSA-179419 | 4.872537e-01 | 0.312 | 0 | 0 |
| Meiotic synapsis | R-HSA-1221632 | 4.872537e-01 | 0.312 | 0 | 0 |
| Translation initiation complex formation | R-HSA-72649 | 4.928485e-01 | 0.307 | 0 | 0 |
| CDK-mediated phosphorylation and removal of Cdc6 | R-HSA-69017 | 4.928485e-01 | 0.307 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176409 | 4.983827e-01 | 0.302 | 0 | 0 |
| Paracetamol ADME | R-HSA-9753281 | 4.983827e-01 | 0.302 | 0 | 0 |
| G alpha (i) signalling events | R-HSA-418594 | 5.029893e-01 | 0.298 | 0 | 0 |
| Ribosomal scanning and start codon recognition | R-HSA-72702 | 5.038568e-01 | 0.298 | 0 | 0 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176814 | 5.038568e-01 | 0.298 | 0 | 0 |
| Intrinsic Pathway for Apoptosis | R-HSA-109606 | 5.038568e-01 | 0.298 | 0 | 0 |
| TNF signaling | R-HSA-75893 | 5.038568e-01 | 0.298 | 0 | 0 |
| Detoxification of Reactive Oxygen Species | R-HSA-3299685 | 5.038568e-01 | 0.298 | 0 | 0 |
| Signaling by FGFR1 | R-HSA-5654736 | 5.038568e-01 | 0.298 | 0 | 0 |
| Ribosome-associated quality control | R-HSA-9948299 | 5.059632e-01 | 0.296 | 0 | 0 |
| Signaling by Hedgehog | R-HSA-5358351 | 5.059632e-01 | 0.296 | 0 | 0 |
| Nuclear Envelope Breakdown | R-HSA-2980766 | 5.092715e-01 | 0.293 | 0 | 0 |
| IRS-mediated signalling | R-HSA-112399 | 5.092715e-01 | 0.293 | 0 | 0 |
| Formation of the beta-catenin:TCF transactivating complex | R-HSA-201722 | 5.146275e-01 | 0.289 | 0 | 0 |
| Activation of the mRNA upon binding of the cap-binding complex and eIFs, and subsequent binding to 43S | R-HSA-72662 | 5.146275e-01 | 0.289 | 0 | 0 |
| Early SARS-CoV-2 Infection Events | R-HSA-9772572 | 5.146275e-01 | 0.289 | 0 | 0 |
| Peroxisomal protein import | R-HSA-9033241 | 5.199253e-01 | 0.284 | 0 | 0 |
| Extension of Telomeres | R-HSA-180786 | 5.199253e-01 | 0.284 | 0 | 0 |
| Assembly of collagen fibrils and other multimeric structures | R-HSA-2022090 | 5.199253e-01 | 0.284 | 0 | 0 |
| Amino acid transport across the plasma membrane | R-HSA-352230 | 5.199253e-01 | 0.284 | 0 | 0 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | R-HSA-5693565 | 5.199253e-01 | 0.284 | 0 | 0 |
| Negative Regulation of CDH1 Gene Transcription | R-HSA-9764725 | 5.251656e-01 | 0.280 | 0 | 0 |
| Formation of paraxial mesoderm | R-HSA-9793380 | 5.303491e-01 | 0.275 | 0 | 0 |
| RNA Polymerase II Transcription Termination | R-HSA-73856 | 5.303491e-01 | 0.275 | 0 | 0 |
| IRS-related events triggered by IGF1R | R-HSA-2428928 | 5.303491e-01 | 0.275 | 0 | 0 |
| Regulation of RUNX2 expression and activity | R-HSA-8939902 | 5.303491e-01 | 0.275 | 0 | 0 |
| PLC beta mediated events | R-HSA-112043 | 5.303491e-01 | 0.275 | 0 | 0 |
| Endogenous sterols | R-HSA-211976 | 5.303491e-01 | 0.275 | 0 | 0 |
| DNA Damage/Telomere Stress Induced Senescence | R-HSA-2559586 | 5.354762e-01 | 0.271 | 0 | 0 |
| Mitochondrial protein import | R-HSA-1268020 | 5.354762e-01 | 0.271 | 0 | 0 |
| Heme signaling | R-HSA-9707616 | 5.354762e-01 | 0.271 | 0 | 0 |
| ER to Golgi Anterograde Transport | R-HSA-199977 | 5.394004e-01 | 0.268 | 0 | 0 |
| Complex I biogenesis | R-HSA-6799198 | 5.405478e-01 | 0.267 | 0 | 0 |
| G1/S DNA Damage Checkpoints | R-HSA-69615 | 5.405478e-01 | 0.267 | 0 | 0 |
| IGF1R signaling cascade | R-HSA-2428924 | 5.455642e-01 | 0.263 | 0 | 0 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | R-HSA-168643 | 5.455642e-01 | 0.263 | 0 | 0 |
| Insulin receptor signalling cascade | R-HSA-74751 | 5.455642e-01 | 0.263 | 0 | 0 |
| Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | R-HSA-2404192 | 5.505262e-01 | 0.259 | 0 | 0 |
| Regulation of PD-L1(CD274) transcription | R-HSA-9909649 | 5.554343e-01 | 0.255 | 0 | 0 |
| Regulation of expression of SLITs and ROBOs | R-HSA-9010553 | 5.555279e-01 | 0.255 | 0 | 0 |
| Protein localization | R-HSA-9609507 | 5.587054e-01 | 0.253 | 0 | 0 |
| DNA Double-Strand Break Repair | R-HSA-5693532 | 5.587054e-01 | 0.253 | 0 | 0 |
| Metabolism of steroid hormones | R-HSA-196071 | 5.602891e-01 | 0.252 | 0 | 0 |
| G-protein mediated events | R-HSA-112040 | 5.602891e-01 | 0.252 | 0 | 0 |
| SLC-mediated transport of amino acids | R-HSA-9958863 | 5.602891e-01 | 0.252 | 0 | 0 |
| DNA Double Strand Break Response | R-HSA-5693606 | 5.602891e-01 | 0.252 | 0 | 0 |
| Epigenetic regulation by WDR5-containing histone modifying complexes | R-HSA-9917777 | 5.618668e-01 | 0.250 | 0 | 0 |
| Influenza Viral RNA Transcription and Replication | R-HSA-168273 | 5.650121e-01 | 0.248 | 0 | 0 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | R-HSA-8936459 | 5.650913e-01 | 0.248 | 0 | 0 |
| Cyclin E associated events during G1/S transition | R-HSA-69202 | 5.745396e-01 | 0.241 | 0 | 0 |
| COPII-mediated vesicle transport | R-HSA-204005 | 5.745396e-01 | 0.241 | 0 | 0 |
| Degradation of beta-catenin by the destruction complex | R-HSA-195253 | 5.745396e-01 | 0.241 | 0 | 0 |
| Regulation of CDH1 Gene Transcription | R-HSA-9764560 | 5.745396e-01 | 0.241 | 0 | 0 |
| Interferon gamma signaling | R-HSA-877300 | 5.774317e-01 | 0.238 | 0 | 0 |
| Hedgehog 'on' state | R-HSA-5632684 | 5.791869e-01 | 0.237 | 0 | 0 |
| Metabolism of cofactors | R-HSA-8978934 | 5.791869e-01 | 0.237 | 0 | 0 |
| Transcriptional and post-translational regulation of MITF-M expression and activity | R-HSA-9856649 | 5.791869e-01 | 0.237 | 0 | 0 |
| Metabolism of porphyrins | R-HSA-189445 | 5.791869e-01 | 0.237 | 0 | 0 |
| Cyclin A:Cdk2-associated events at S phase entry | R-HSA-69656 | 5.837838e-01 | 0.234 | 0 | 0 |
| Nuclear Events (kinase and transcription factor activation) | R-HSA-198725 | 5.837838e-01 | 0.234 | 0 | 0 |
| Cellular responses to stress | R-HSA-2262752 | 5.870781e-01 | 0.231 | 0 | 0 |
| Transport of Mature mRNA derived from an Intron-Containing Transcript | R-HSA-159236 | 5.883307e-01 | 0.230 | 0 | 0 |
| Switching of origins to a post-replicative state | R-HSA-69052 | 5.883307e-01 | 0.230 | 0 | 0 |
| Ca2+ pathway | R-HSA-4086398 | 5.883307e-01 | 0.230 | 0 | 0 |
| Separation of Sister Chromatids | R-HSA-2467813 | 5.925915e-01 | 0.227 | 0 | 0 |
| G2/M DNA damage checkpoint | R-HSA-69473 | 5.928283e-01 | 0.227 | 0 | 0 |
| Protein ubiquitination | R-HSA-8852135 | 5.972769e-01 | 0.224 | 0 | 0 |
| DNA Repair | R-HSA-73894 | 5.984714e-01 | 0.223 | 0 | 0 |
| Developmental Cell Lineages | R-HSA-9734767 | 5.994426e-01 | 0.222 | 0 | 0 |
| G alpha (q) signalling events | R-HSA-416476 | 6.018300e-01 | 0.221 | 0 | 0 |
| Gene expression (Transcription) | R-HSA-74160 | 6.023398e-01 | 0.220 | 0 | 0 |
| Nuclear Receptor transcription pathway | R-HSA-383280 | 6.103350e-01 | 0.214 | 0 | 0 |
| Cholesterol biosynthesis | R-HSA-191273 | 6.103350e-01 | 0.214 | 0 | 0 |
| Integrin cell surface interactions | R-HSA-216083 | 6.103350e-01 | 0.214 | 0 | 0 |
| Metabolic disorders of biological oxidation enzymes | R-HSA-5579029 | 6.145935e-01 | 0.211 | 0 | 0 |
| Transcriptional Regulation by TP53 | R-HSA-3700989 | 6.157107e-01 | 0.211 | 0 | 0 |
| G alpha (s) signalling events | R-HSA-418555 | 6.160020e-01 | 0.210 | 0 | 0 |
| Signaling by MET | R-HSA-6806834 | 6.188057e-01 | 0.208 | 0 | 0 |
| Nuclear Envelope (NE) Reassembly | R-HSA-2995410 | 6.188057e-01 | 0.208 | 0 | 0 |
| Processing of DNA double-strand break ends | R-HSA-5693607 | 6.229721e-01 | 0.206 | 0 | 0 |
| Amyloid fiber formation | R-HSA-977225 | 6.229721e-01 | 0.206 | 0 | 0 |
| Transport of Mature Transcript to Cytoplasm | R-HSA-72202 | 6.270932e-01 | 0.203 | 0 | 0 |
| Senescence-Associated Secretory Phenotype (SASP) | R-HSA-2559582 | 6.270932e-01 | 0.203 | 0 | 0 |
| Influenza Infection | R-HSA-168255 | 6.383745e-01 | 0.195 | 0 | 0 |
| Protein-protein interactions at synapses | R-HSA-6794362 | 6.391898e-01 | 0.194 | 0 | 0 |
| MAPK6/MAPK4 signaling | R-HSA-5687128 | 6.391898e-01 | 0.194 | 0 | 0 |
| Post NMDA receptor activation events | R-HSA-438064 | 6.508961e-01 | 0.186 | 0 | 0 |
| Peptide chain elongation | R-HSA-156902 | 6.547136e-01 | 0.184 | 0 | 0 |
| Diseases of programmed cell death | R-HSA-9645723 | 6.547136e-01 | 0.184 | 0 | 0 |
| ER-Phagosome pathway | R-HSA-1236974 | 6.584897e-01 | 0.181 | 0 | 0 |
| Bacterial Infection Pathways | R-HSA-9824439 | 6.596313e-01 | 0.181 | 0 | 0 |
| PELO:HBS1L and ABCE1 dissociate a ribosome on a non-stop mRNA | R-HSA-9954714 | 6.659190e-01 | 0.177 | 0 | 0 |
| Pre-NOTCH Transcription and Translation | R-HSA-1912408 | 6.659190e-01 | 0.177 | 0 | 0 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | R-HSA-975956 | 6.695732e-01 | 0.174 | 0 | 0 |
| Eukaryotic Translation Elongation | R-HSA-156842 | 6.731876e-01 | 0.172 | 0 | 0 |
| Signaling by Insulin receptor | R-HSA-74752 | 6.731876e-01 | 0.172 | 0 | 0 |
| Signaling by WNT | R-HSA-195721 | 6.773709e-01 | 0.169 | 0 | 0 |
| Mitochondrial protein degradation | R-HSA-9837999 | 6.802990e-01 | 0.167 | 0 | 0 |
| Collagen formation | R-HSA-1474290 | 6.802990e-01 | 0.167 | 0 | 0 |
| ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ribosome stalled on a no-go mRNA | R-HSA-9954716 | 6.837968e-01 | 0.165 | 0 | 0 |
| Mitochondrial Fatty Acid Beta-Oxidation | R-HSA-77289 | 6.837968e-01 | 0.165 | 0 | 0 |
| Eukaryotic Translation Termination | R-HSA-72764 | 6.872565e-01 | 0.163 | 0 | 0 |
| Formation of a pool of free 40S subunits | R-HSA-72689 | 6.872565e-01 | 0.163 | 0 | 0 |
| COPI-mediated anterograde transport | R-HSA-6807878 | 6.906785e-01 | 0.161 | 0 | 0 |
| Signaling by TGF-beta Receptor Complex | R-HSA-170834 | 6.940634e-01 | 0.159 | 0 | 0 |
| Telomere Maintenance | R-HSA-157579 | 6.940634e-01 | 0.159 | 0 | 0 |
| Transport to the Golgi and subsequent modification | R-HSA-948021 | 6.970164e-01 | 0.157 | 0 | 0 |
| Post-translational protein phosphorylation | R-HSA-8957275 | 6.974114e-01 | 0.157 | 0 | 0 |
| Glycerophospholipid biosynthesis | R-HSA-1483206 | 6.993793e-01 | 0.155 | 0 | 0 |
| Selenocysteine synthesis | R-HSA-2408557 | 7.072384e-01 | 0.150 | 0 | 0 |
| Activation of NMDA receptors and postsynaptic events | R-HSA-442755 | 7.104430e-01 | 0.148 | 0 | 0 |
| Viral mRNA Translation | R-HSA-192823 | 7.136127e-01 | 0.147 | 0 | 0 |
| Mitochondrial ribosome-associated quality control | R-HSA-9937383 | 7.136127e-01 | 0.147 | 0 | 0 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | R-HSA-9633012 | 7.167480e-01 | 0.145 | 0 | 0 |
| Toll Like Receptor 3 (TLR3) Cascade | R-HSA-168164 | 7.229164e-01 | 0.141 | 0 | 0 |
| Platelet homeostasis | R-HSA-418346 | 7.259504e-01 | 0.139 | 0 | 0 |
| Translation | R-HSA-72766 | 7.272619e-01 | 0.138 | 0 | 0 |
| SRP-dependent cotranslational protein targeting to membrane | R-HSA-1799339 | 7.289513e-01 | 0.137 | 0 | 0 |
| Synthesis of DNA | R-HSA-69239 | 7.289513e-01 | 0.137 | 0 | 0 |
| Gene Silencing by RNA | R-HSA-211000 | 7.289513e-01 | 0.137 | 0 | 0 |
| Antigen processing-Cross presentation | R-HSA-1236975 | 7.319195e-01 | 0.136 | 0 | 0 |
| TRAF6 mediated induction of NFkB and MAP kinases upon TLR7/8 or 9 activation | R-HSA-975138 | 7.319195e-01 | 0.136 | 0 | 0 |
| DNA Replication Pre-Initiation | R-HSA-69002 | 7.348555e-01 | 0.134 | 0 | 0 |
| MyD88 dependent cascade initiated on endosome | R-HSA-975155 | 7.348555e-01 | 0.134 | 0 | 0 |
| Extracellular matrix organization | R-HSA-1474244 | 7.401248e-01 | 0.131 | 0 | 0 |
| Inositol phosphate metabolism | R-HSA-1483249 | 7.434728e-01 | 0.129 | 0 | 0 |
| Pre-NOTCH Expression and Processing | R-HSA-1912422 | 7.462829e-01 | 0.127 | 0 | 0 |
| Toll Like Receptor 7/8 (TLR7/8) Cascade | R-HSA-168181 | 7.462829e-01 | 0.127 | 0 | 0 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | R-HSA-381426 | 7.518115e-01 | 0.124 | 0 | 0 |
| HIV Infection | R-HSA-162906 | 7.536511e-01 | 0.123 | 0 | 0 |
| Toll Like Receptor 9 (TLR9) Cascade | R-HSA-168138 | 7.545308e-01 | 0.122 | 0 | 0 |
| Mitochondrial biogenesis | R-HSA-1592230 | 7.625121e-01 | 0.118 | 0 | 0 |
| Peptide hormone metabolism | R-HSA-2980736 | 7.625121e-01 | 0.118 | 0 | 0 |
| MyD88:MAL(TIRAP) cascade initiated on plasma membrane | R-HSA-166058 | 7.676890e-01 | 0.115 | 0 | 0 |
| Toll Like Receptor TLR6:TLR2 Cascade | R-HSA-168188 | 7.676890e-01 | 0.115 | 0 | 0 |
| Mitotic Prophase | R-HSA-68875 | 7.702353e-01 | 0.113 | 0 | 0 |
| Chromosome Maintenance | R-HSA-73886 | 7.727538e-01 | 0.112 | 0 | 0 |
| Toll Like Receptor TLR1:TLR2 Cascade | R-HSA-168179 | 7.752448e-01 | 0.111 | 0 | 0 |
| Toll Like Receptor 2 (TLR2) Cascade | R-HSA-181438 | 7.752448e-01 | 0.111 | 0 | 0 |
| Formation of the cornified envelope | R-HSA-6809371 | 7.801457e-01 | 0.108 | 0 | 0 |
| Beta-catenin independent WNT signaling | R-HSA-3858494 | 8.136689e-01 | 0.090 | 0 | 0 |
| Mitochondrial translation | R-HSA-5368287 | 8.177362e-01 | 0.087 | 0 | 0 |
| Biosynthesis of specialized proresolving mediators (SPMs) | R-HSA-9018678 | 8.294161e-01 | 0.081 | 0 | 0 |
| S Phase | R-HSA-69242 | 8.385786e-01 | 0.076 | 0 | 0 |
| Phase I - Functionalization of compounds | R-HSA-211945 | 8.387262e-01 | 0.076 | 0 | 0 |
| Gastrulation | R-HSA-9758941 | 8.403515e-01 | 0.076 | 0 | 0 |
| Binding and Uptake of Ligands by Scavenger Receptors | R-HSA-2173782 | 8.421050e-01 | 0.075 | 0 | 0 |
| Arachidonate metabolism | R-HSA-2142753 | 8.455548e-01 | 0.073 | 0 | 0 |
| Interleukin-1 family signaling | R-HSA-446652 | 8.455548e-01 | 0.073 | 0 | 0 |
| DNA Replication | R-HSA-69306 | 8.472515e-01 | 0.072 | 0 | 0 |
| Cellular response to starvation | R-HSA-9711097 | 8.554610e-01 | 0.068 | 0 | 0 |
| Signaling by TGFB family members | R-HSA-9006936 | 8.586206e-01 | 0.066 | 0 | 0 |
| Selenoamino acid metabolism | R-HSA-2408522 | 8.647352e-01 | 0.063 | 0 | 0 |
| Asparagine N-linked glycosylation | R-HSA-446203 | 8.650209e-01 | 0.063 | 0 | 0 |
| Cytochrome P450 - arranged by substrate type | R-HSA-211897 | 8.691480e-01 | 0.061 | 0 | 0 |
| SLC transporter disorders | R-HSA-5619102 | 8.691480e-01 | 0.061 | 0 | 0 |
| Major pathway of rRNA processing in the nucleolus and cytosol | R-HSA-6791226 | 8.748097e-01 | 0.058 | 0 | 0 |
| Ub-specific processing proteases | R-HSA-5689880 | 8.788955e-01 | 0.056 | 0 | 0 |
| Respiratory electron transport | R-HSA-611105 | 8.854127e-01 | 0.053 | 0 | 0 |
| Cellular Senescence | R-HSA-2559583 | 8.879208e-01 | 0.052 | 0 | 0 |
| Epigenetic regulation of gene expression | R-HSA-212165 | 8.907840e-01 | 0.050 | 0 | 0 |
| Metabolism of steroids | R-HSA-8957322 | 8.917418e-01 | 0.050 | 0 | 0 |
| Peptide ligand-binding receptors | R-HSA-375276 | 8.951223e-01 | 0.048 | 0 | 0 |
| rRNA processing in the nucleus and cytosol | R-HSA-8868773 | 8.974190e-01 | 0.047 | 0 | 0 |
| Aerobic respiration and respiratory electron transport | R-HSA-1428517 | 9.068804e-01 | 0.042 | 0 | 0 |
| Keratinization | R-HSA-6805567 | 9.168905e-01 | 0.038 | 0 | 0 |
| Neurotransmitter receptors and postsynaptic signal transmission | R-HSA-112314 | 9.222394e-01 | 0.035 | 0 | 0 |
| Neddylation | R-HSA-8951664 | 9.296275e-01 | 0.032 | 0 | 0 |
| rRNA processing | R-HSA-72312 | 9.377158e-01 | 0.028 | 0 | 0 |
| Biological oxidations | R-HSA-211859 | 9.386505e-01 | 0.027 | 0 | 0 |
| Chromatin modifying enzymes | R-HSA-3247509 | 9.390838e-01 | 0.027 | 0 | 0 |
| Phase II - Conjugation of compounds | R-HSA-156580 | 9.423744e-01 | 0.026 | 0 | 0 |
| Signaling by NOTCH | R-HSA-157118 | 9.430110e-01 | 0.025 | 0 | 0 |
| SLC-mediated transmembrane transport | R-HSA-425407 | 9.444328e-01 | 0.025 | 0 | 0 |
| Chromatin organization | R-HSA-4839726 | 9.484347e-01 | 0.023 | 0 | 0 |
| Fatty acid metabolism | R-HSA-8978868 | 9.493265e-01 | 0.023 | 0 | 0 |
| Diseases of metabolism | R-HSA-5668914 | 9.579140e-01 | 0.019 | 0 | 0 |
| Neuronal System | R-HSA-112316 | 9.713838e-01 | 0.013 | 0 | 0 |
| Metabolism of proteins | R-HSA-392499 | 9.765231e-01 | 0.010 | 0 | 0 |
| Transmission across Chemical Synapses | R-HSA-112315 | 9.773901e-01 | 0.010 | 0 | 0 |
| Metabolism of vitamins and cofactors | R-HSA-196854 | 9.857048e-01 | 0.006 | 0 | 0 |
| Transport of small molecules | R-HSA-382551 | 9.866053e-01 | 0.006 | 0 | 0 |
| Metabolism of lipids | R-HSA-556833 | 9.868104e-01 | 0.006 | 0 | 0 |
| Class I MHC mediated antigen processing & presentation | R-HSA-983169 | 9.885745e-01 | 0.005 | 0 | 0 |
| Class A/1 (Rhodopsin-like receptors) | R-HSA-373076 | 9.899005e-01 | 0.004 | 0 | 0 |
| Post-translational protein modification | R-HSA-597592 | 9.905745e-01 | 0.004 | 0 | 0 |
| Metabolism of amino acids and derivatives | R-HSA-71291 | 9.933520e-01 | 0.003 | 0 | 0 |
| GPCR ligand binding | R-HSA-500792 | 9.988825e-01 | 0.000 | 0 | 0 |
| Sensory Perception | R-HSA-9709957 | 9.999233e-01 | 0.000 | 0 | 0 |
| Metabolism | R-HSA-1430728 | 9.999993e-01 | 0.000 | 0 | 0 |
| FCERI mediated NF-kB activation | R-HSA-2871837 | 1.000000e+00 | 0.000 | 1 | 1 |
| CD22 mediated BCR regulation | R-HSA-5690714 | 1.000000e+00 | 0.000 | 1 | 1 |
| Erythropoietin activates Phosphoinositide-3-kinase (PI3K) | R-HSA-9027276 | 1.000000e+00 | 0.000 | 1 | 1 |
| Erythropoietin activates STAT5 | R-HSA-9027283 | 1.000000e+00 | 0.000 | 1 | 1 |
| Signaling by CSF3 (G-CSF) | R-HSA-9674555 | 1.000000e+00 | 0.000 | 1 | 1 |
| Inactivation of CSF3 (G-CSF) signaling | R-HSA-9705462 | 1.000000e+00 | 0.000 | 1 | 1 |
| Growth hormone receptor signaling | R-HSA-982772 | 1.000000e+00 | 0.000 | 1 | 1 |
Top15 pathways (red highlights are reference pathways)
Compared with reference pathways
Motif of predicted substrate sequence
Reactome pathways of predicted substrates
Download
| name | reactome_id | p | -log10p | ref_path | ref_path_lowest |
|---|---|---|---|---|---|
| G2/M DNA damage checkpoint | R-HSA-69473 | 1.110223e-16 | 15.955 | 0 | 0 |
| G2/M Checkpoints | R-HSA-69481 | 1.110223e-16 | 15.955 | 0 | 0 |
| Regulation of CDH1 Expression and Function | R-HSA-9764265 | 5.551115e-16 | 15.256 | 0 | 0 |
| Regulation of Expression and Function of Type I Classical Cadherins | R-HSA-9764274 | 5.551115e-16 | 15.256 | 0 | 0 |
| Translocation of SLC2A4 (GLUT4) to the plasma membrane | R-HSA-1445148 | 1.776357e-15 | 14.750 | 0 | 0 |
| Adherens junctions interactions | R-HSA-418990 | 3.885781e-15 | 14.411 | 0 | 0 |
| Regulation of Homotypic Cell-Cell Adhesion | R-HSA-9759476 | 5.107026e-15 | 14.292 | 0 | 0 |
| Cell Cycle | R-HSA-1640170 | 6.439294e-15 | 14.191 | 1 | 0 |
| Cell-Cell communication | R-HSA-1500931 | 9.547918e-15 | 14.020 | 0 | 0 |
| Cell junction organization | R-HSA-446728 | 4.751755e-14 | 13.323 | 0 | 0 |
| Viral Infection Pathways | R-HSA-9824446 | 4.696243e-14 | 13.328 | 0 | 0 |
| Cell-cell junction organization | R-HSA-421270 | 5.706546e-14 | 13.244 | 0 | 0 |
| Replacement of protamines by nucleosomes in the male pronucleus | R-HSA-9821993 | 6.883383e-14 | 13.162 | 0 | 0 |
| Cell Cycle, Mitotic | R-HSA-69278 | 8.593126e-14 | 13.066 | 1 | 0 |
| Packaging Of Telomere Ends | R-HSA-171306 | 1.910694e-13 | 12.719 | 0 | 0 |
| RNA Polymerase I Promoter Opening | R-HSA-73728 | 1.910694e-13 | 12.719 | 0 | 0 |
| DNA methylation | R-HSA-5334118 | 3.581579e-13 | 12.446 | 0 | 0 |
| M Phase | R-HSA-68886 | 5.834222e-13 | 12.234 | 0 | 0 |
| Cell Cycle Checkpoints | R-HSA-69620 | 8.175682e-13 | 12.087 | 0 | 0 |
| Recognition and association of DNA glycosylase with site containing an affected purine | R-HSA-110330 | 8.602008e-13 | 12.065 | 0 | 0 |
| Assembly of the ORC complex at the origin of replication | R-HSA-68616 | 1.133871e-12 | 11.945 | 0 | 0 |
| Condensation of Prophase Chromosomes | R-HSA-2299718 | 1.636025e-12 | 11.786 | 0 | 0 |
| Regulation of endogenous retroelements by the Human Silencing Hub (HUSH) complex | R-HSA-9843970 | 1.928679e-12 | 11.715 | 0 | 0 |
| Recognition and association of DNA glycosylase with site containing an affected pyrimidine | R-HSA-110328 | 1.928679e-12 | 11.715 | 0 | 0 |
| Cellular responses to stress | R-HSA-2262752 | 2.919109e-12 | 11.535 | 0 | 0 |
| PRC2 methylates histones and DNA | R-HSA-212300 | 3.195888e-12 | 11.495 | 0 | 0 |
| SIRT1 negatively regulates rRNA expression | R-HSA-427359 | 4.076850e-12 | 11.390 | 0 | 0 |
| Cleavage of the damaged purine | R-HSA-110331 | 4.076850e-12 | 11.390 | 0 | 0 |
| Meiotic recombination | R-HSA-912446 | 4.516165e-12 | 11.345 | 0 | 0 |
| Depurination | R-HSA-73927 | 5.171086e-12 | 11.286 | 0 | 0 |
| Regulation of T cell activation by CD28 family | R-HSA-388841 | 5.786038e-12 | 11.238 | 1 | 0 |
| Infectious disease | R-HSA-5663205 | 6.101120e-12 | 11.215 | 1 | 0 |
| B-WICH complex positively regulates rRNA expression | R-HSA-5250924 | 6.611267e-12 | 11.180 | 0 | 0 |
| Inhibition of DNA recombination at telomere | R-HSA-9670095 | 8.186785e-12 | 11.087 | 0 | 0 |
| ERCC6 (CSB) and EHMT2 (G9a) positively regulate rRNA expression | R-HSA-427389 | 8.186785e-12 | 11.087 | 0 | 0 |
| Activated PKN1 stimulates transcription of AR (androgen receptor) regulated genes KLK2 and KLK3 | R-HSA-5625886 | 1.022327e-11 | 10.990 | 0 | 0 |
| Chromatin modifications during the maternal to zygotic transition (MZT) | R-HSA-9821002 | 1.022327e-11 | 10.990 | 0 | 0 |
| Cleavage of the damaged pyrimidine | R-HSA-110329 | 1.571820e-11 | 10.804 | 0 | 0 |
| Depyrimidination | R-HSA-73928 | 1.571820e-11 | 10.804 | 0 | 0 |
| Defective pyroptosis | R-HSA-9710421 | 1.935996e-11 | 10.713 | 0 | 0 |
| Regulation of endogenous retroelements by Piwi-interacting RNAs (piRNAs) | R-HSA-9845323 | 2.278677e-11 | 10.642 | 0 | 0 |
| Cellular responses to stimuli | R-HSA-8953897 | 2.475609e-11 | 10.606 | 0 | 0 |
| Chk1/Chk2(Cds1) mediated inactivation of Cyclin B:Cdk1 complex | R-HSA-75035 | 2.679601e-11 | 10.572 | 0 | 0 |
| Nucleosome assembly | R-HSA-774815 | 2.900435e-11 | 10.538 | 0 | 0 |
| Deposition of new CENPA-containing nucleosomes at the centromere | R-HSA-606279 | 2.900435e-11 | 10.538 | 0 | 0 |
| DNA Damage/Telomere Stress Induced Senescence | R-HSA-2559586 | 3.166190e-11 | 10.499 | 0 | 0 |
| Transcriptional regulation of granulopoiesis | R-HSA-9616222 | 3.166190e-11 | 10.499 | 0 | 0 |
| Senescence-Associated Secretory Phenotype (SASP) | R-HSA-2559582 | 3.792411e-11 | 10.421 | 0 | 0 |
| Nonhomologous End-Joining (NHEJ) | R-HSA-5693571 | 5.166456e-11 | 10.287 | 0 | 0 |
| Co-inhibition by PD-1 | R-HSA-389948 | 6.021461e-11 | 10.220 | 0 | 0 |
| Activation of BAD and translocation to mitochondria | R-HSA-111447 | 6.403456e-11 | 10.194 | 0 | 0 |
| SARS-CoV-2 targets host intracellular signalling and regulatory pathways | R-HSA-9755779 | 6.403456e-11 | 10.194 | 0 | 0 |
| Diseases of programmed cell death | R-HSA-9645723 | 9.397860e-11 | 10.027 | 0 | 0 |
| RNA Polymerase I Promoter Escape | R-HSA-73772 | 1.062633e-10 | 9.974 | 0 | 0 |
| DNA Replication Pre-Initiation | R-HSA-69002 | 1.168026e-10 | 9.933 | 0 | 0 |
| Positive epigenetic regulation of rRNA expression | R-HSA-5250913 | 1.241425e-10 | 9.906 | 0 | 0 |
| Meiotic synapsis | R-HSA-1221632 | 1.262546e-10 | 9.899 | 0 | 0 |
| Base-Excision Repair, AP Site Formation | R-HSA-73929 | 1.495638e-10 | 9.825 | 0 | 0 |
| Signal Transduction | R-HSA-162582 | 1.644540e-10 | 9.784 | 1 | 0 |
| HDACs deacetylate histones | R-HSA-3214815 | 1.766701e-10 | 9.753 | 0 | 0 |
| Assembly of the pre-replicative complex | R-HSA-68867 | 1.937414e-10 | 9.713 | 0 | 0 |
| Formation of the beta-catenin:TCF transactivating complex | R-HSA-201722 | 2.864826e-10 | 9.543 | 0 | 0 |
| Recruitment and ATM-mediated phosphorylation of repair and signaling proteins at DNA double strand breaks | R-HSA-5693565 | 3.348398e-10 | 9.475 | 0 | 0 |
| HCMV Early Events | R-HSA-9609690 | 3.759474e-10 | 9.425 | 0 | 0 |
| Negative Regulation of CDH1 Gene Transcription | R-HSA-9764725 | 3.904018e-10 | 9.408 | 0 | 0 |
| Processing of DNA double-strand break ends | R-HSA-5693607 | 4.720689e-10 | 9.326 | 0 | 0 |
| Regulation of PD-L1(CD274) expression | R-HSA-9909648 | 5.587627e-10 | 9.253 | 0 | 0 |
| RUNX1 regulates transcription of genes involved in differentiation of HSCs | R-HSA-8939236 | 6.830597e-10 | 9.166 | 0 | 0 |
| Meiosis | R-HSA-1500620 | 7.703593e-10 | 9.113 | 0 | 0 |
| EPH-ephrin mediated repulsion of cells | R-HSA-3928665 | 8.261047e-10 | 9.083 | 1 | 1 |
| Axon guidance | R-HSA-422475 | 8.869482e-10 | 9.052 | 1 | 0 |
| Regulation of PD-L1(CD274) transcription | R-HSA-9909649 | 9.351059e-10 | 9.029 | 0 | 0 |
| DNA Double Strand Break Response | R-HSA-5693606 | 1.073707e-09 | 8.969 | 0 | 0 |
| RUNX1 regulates genes involved in megakaryocyte differentiation and platelet function | R-HSA-8936459 | 1.230442e-09 | 8.910 | 0 | 0 |
| TCF dependent signaling in response to WNT | R-HSA-201681 | 1.233575e-09 | 8.909 | 0 | 0 |
| Disease | R-HSA-1643685 | 1.561447e-09 | 8.806 | 1 | 0 |
| Regulation of endogenous retroelements by KRAB-ZFP proteins | R-HSA-9843940 | 1.606766e-09 | 8.794 | 0 | 0 |
| Adaptive Immune System | R-HSA-1280218 | 1.576458e-09 | 8.802 | 1 | 0 |
| Pre-NOTCH Transcription and Translation | R-HSA-1912408 | 1.722468e-09 | 8.764 | 0 | 0 |
| Regulation of CDH1 Gene Transcription | R-HSA-9764560 | 1.606766e-09 | 8.794 | 0 | 0 |
| NoRC negatively regulates rRNA expression | R-HSA-427413 | 1.831092e-09 | 8.737 | 0 | 0 |
| Transcriptional regulation by small RNAs | R-HSA-5578749 | 2.083062e-09 | 8.681 | 0 | 0 |
| EPH-Ephrin signaling | R-HSA-2682334 | 2.143582e-09 | 8.669 | 1 | 1 |
| SARS-CoV-1 targets host intracellular signalling and regulatory pathways | R-HSA-9735871 | 2.558498e-09 | 8.592 | 0 | 0 |
| Developmental Biology | R-HSA-1266738 | 2.914589e-09 | 8.535 | 1 | 0 |
| Nervous system development | R-HSA-9675108 | 3.265700e-09 | 8.486 | 1 | 0 |
| RNA Polymerase I Promoter Clearance | R-HSA-73854 | 3.430728e-09 | 8.465 | 0 | 0 |
| Telomere Maintenance | R-HSA-157579 | 4.021466e-09 | 8.396 | 0 | 0 |
| RNA Polymerase I Transcription | R-HSA-73864 | 4.361123e-09 | 8.360 | 0 | 0 |
| Mitotic Prophase | R-HSA-68875 | 4.418729e-09 | 8.355 | 0 | 0 |
| HATs acetylate histones | R-HSA-3214847 | 4.918118e-09 | 8.308 | 0 | 0 |
| Negative epigenetic regulation of rRNA expression | R-HSA-5250941 | 5.510949e-09 | 8.259 | 0 | 0 |
| Amyloid fiber formation | R-HSA-977225 | 6.181701e-09 | 8.209 | 0 | 0 |
| Signaling by NOTCH | R-HSA-157118 | 6.218683e-09 | 8.206 | 0 | 0 |
| Regulation of endogenous retroelements | R-HSA-9842860 | 6.602514e-09 | 8.180 | 0 | 0 |
| Activation of BH3-only proteins | R-HSA-114452 | 9.079276e-09 | 8.042 | 0 | 0 |
| DNA Replication | R-HSA-69306 | 9.223462e-09 | 8.035 | 0 | 0 |
| HCMV Infection | R-HSA-9609646 | 1.074749e-08 | 7.969 | 0 | 0 |
| Gene Silencing by RNA | R-HSA-211000 | 1.160633e-08 | 7.935 | 0 | 0 |
| Regulation of localization of FOXO transcription factors | R-HSA-9614399 | 1.490575e-08 | 7.827 | 0 | 0 |
| Post-chaperonin tubulin folding pathway | R-HSA-389977 | 1.652987e-08 | 7.782 | 0 | 0 |
| Base Excision Repair | R-HSA-73884 | 1.814756e-08 | 7.741 | 0 | 0 |
| Pre-NOTCH Expression and Processing | R-HSA-1912422 | 1.978866e-08 | 7.704 | 0 | 0 |
| Estrogen-dependent gene expression | R-HSA-9018519 | 2.069364e-08 | 7.684 | 0 | 0 |
| HDR through Homologous Recombination (HRR) or Single Strand Annealing (SSA) | R-HSA-5693567 | 2.156935e-08 | 7.666 | 0 | 0 |
| E3 ubiquitin ligases ubiquitinate target proteins | R-HSA-8866654 | 3.013366e-08 | 7.521 | 0 | 0 |
| L1CAM interactions | R-HSA-373760 | 3.021957e-08 | 7.520 | 0 | 0 |
| Homology Directed Repair | R-HSA-5693538 | 3.561592e-08 | 7.448 | 0 | 0 |
| Non-integrin membrane-ECM interactions | R-HSA-3000171 | 3.888205e-08 | 7.410 | 0 | 0 |
| Chromosome Maintenance | R-HSA-73886 | 4.533629e-08 | 7.344 | 0 | 0 |
| Epigenetic regulation of adipogenesis genes by MLL3 and MLL4 complexes | R-HSA-9851695 | 6.690383e-08 | 7.175 | 0 | 0 |
| MLL4 and MLL3 complexes regulate expression of PPARG target genes in adipogenesis and hepatic steatosis | R-HSA-9841922 | 6.690383e-08 | 7.175 | 0 | 0 |
| Epigenetic regulation of gene expression by MLL3 and MLL4 complexes | R-HSA-9818564 | 6.690383e-08 | 7.175 | 0 | 0 |
| Oxidative Stress Induced Senescence | R-HSA-2559580 | 6.812800e-08 | 7.167 | 0 | 0 |
| Activation of anterior HOX genes in hindbrain development during early embryogenesis | R-HSA-5617472 | 8.835061e-08 | 7.054 | 0 | 0 |
| Activation of HOX genes during differentiation | R-HSA-5619507 | 8.835061e-08 | 7.054 | 0 | 0 |
| Reproduction | R-HSA-1474165 | 1.045969e-07 | 6.980 | 0 | 0 |
| The role of GTSE1 in G2/M progression after G2 checkpoint | R-HSA-8852276 | 1.098779e-07 | 6.959 | 0 | 0 |
| Signaling by WNT | R-HSA-195721 | 1.102397e-07 | 6.958 | 0 | 0 |
| Gap junction trafficking | R-HSA-190828 | 1.482590e-07 | 6.829 | 0 | 0 |
| Recruitment of NuMA to mitotic centrosomes | R-HSA-380320 | 1.619959e-07 | 6.790 | 0 | 0 |
| ESR-mediated signaling | R-HSA-8939211 | 2.130492e-07 | 6.672 | 0 | 0 |
| Recycling pathway of L1 | R-HSA-437239 | 2.258315e-07 | 6.646 | 0 | 0 |
| TP53 Regulates Metabolic Genes | R-HSA-5628897 | 2.329834e-07 | 6.633 | 0 | 0 |
| Protein folding | R-HSA-391251 | 2.554894e-07 | 6.593 | 0 | 0 |
| Gap junction trafficking and regulation | R-HSA-157858 | 2.949913e-07 | 6.530 | 0 | 0 |
| Cellular Senescence | R-HSA-2559583 | 4.082251e-07 | 6.389 | 0 | 0 |
| Protein ubiquitination | R-HSA-8852135 | 4.507130e-07 | 6.346 | 0 | 0 |
| Maternal to zygotic transition (MZT) | R-HSA-9816359 | 4.519423e-07 | 6.345 | 0 | 0 |
| DNA Double-Strand Break Repair | R-HSA-5693532 | 5.503415e-07 | 6.259 | 0 | 0 |
| G2/M Transition | R-HSA-69275 | 5.674863e-07 | 6.246 | 0 | 0 |
| Epigenetic regulation by WDR5-containing histone modifying complexes | R-HSA-9917777 | 5.846780e-07 | 6.233 | 0 | 0 |
| Signaling by Receptor Tyrosine Kinases | R-HSA-9006934 | 5.954939e-07 | 6.225 | 1 | 0 |
| Mitotic G2-G2/M phases | R-HSA-453274 | 6.317593e-07 | 6.199 | 0 | 0 |
| Intrinsic Pathway for Apoptosis | R-HSA-109606 | 6.982404e-07 | 6.156 | 0 | 0 |
| Transcriptional regulation by RUNX1 | R-HSA-8878171 | 7.373508e-07 | 6.132 | 0 | 0 |
| Regulation of CDH1 Function | R-HSA-9764561 | 7.831379e-07 | 6.106 | 0 | 0 |
| Chromatin modifying enzymes | R-HSA-3247509 | 1.069940e-06 | 5.971 | 0 | 0 |
| Immune System | R-HSA-168256 | 1.141885e-06 | 5.942 | 1 | 0 |
| VEGFR2 mediated vascular permeability | R-HSA-5218920 | 1.286569e-06 | 5.891 | 0 | 0 |
| Selective autophagy | R-HSA-9663891 | 1.608009e-06 | 5.794 | 0 | 0 |
| Ub-specific processing proteases | R-HSA-5689880 | 1.811892e-06 | 5.742 | 0 | 0 |
| Chromatin organization | R-HSA-4839726 | 2.072721e-06 | 5.683 | 0 | 0 |
| VEGFA-VEGFR2 Pathway | R-HSA-4420097 | 2.075341e-06 | 5.683 | 0 | 0 |
| EPHA-mediated growth cone collapse | R-HSA-3928663 | 2.151836e-06 | 5.667 | 1 | 1 |
| HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand | R-HSA-3371497 | 2.469951e-06 | 5.607 | 0 | 0 |
| Activation of AMPK downstream of NMDARs | R-HSA-9619483 | 2.550732e-06 | 5.593 | 0 | 0 |
| Deubiquitination | R-HSA-5688426 | 2.666831e-06 | 5.574 | 0 | 0 |
| Cooperation of Prefoldin and TriC/CCT in actin and tubulin folding | R-HSA-389958 | 4.122897e-06 | 5.385 | 0 | 0 |
| Signaling by VEGF | R-HSA-194138 | 4.242462e-06 | 5.372 | 0 | 0 |
| Autophagy | R-HSA-9612973 | 4.423393e-06 | 5.354 | 0 | 0 |
| Formation of the dystrophin-glycoprotein complex (DGC) | R-HSA-9913351 | 4.122897e-06 | 5.385 | 0 | 0 |
| SARS-CoV-2-host interactions | R-HSA-9705683 | 4.491242e-06 | 5.348 | 0 | 0 |
| Mitotic Prometaphase | R-HSA-68877 | 4.926255e-06 | 5.307 | 0 | 0 |
| Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane | R-HSA-190840 | 5.353829e-06 | 5.271 | 0 | 0 |
| SARS-CoV Infections | R-HSA-9679506 | 6.512391e-06 | 5.186 | 0 | 0 |
| Transport of connexons to the plasma membrane | R-HSA-190872 | 6.627391e-06 | 5.179 | 0 | 0 |
| Generic Transcription Pathway | R-HSA-212436 | 7.338228e-06 | 5.134 | 0 | 0 |
| Transcriptional Regulation by TP53 | R-HSA-3700989 | 8.240509e-06 | 5.084 | 0 | 0 |
| RNA Polymerase II Transcription | R-HSA-73857 | 8.644852e-06 | 5.063 | 0 | 0 |
| HSF1 activation | R-HSA-3371511 | 9.621004e-06 | 5.017 | 0 | 0 |
| Chaperonin-mediated protein folding | R-HSA-390466 | 1.329866e-05 | 4.876 | 0 | 0 |
| Aggrephagy | R-HSA-9646399 | 1.582294e-05 | 4.801 | 0 | 0 |
| Loss of proteins required for interphase microtubule organization from the centrosome | R-HSA-380284 | 1.613730e-05 | 4.792 | 0 | 0 |
| Loss of Nlp from mitotic centrosomes | R-HSA-380259 | 1.613730e-05 | 4.792 | 0 | 0 |
| Prefoldin mediated transfer of substrate to CCT/TriC | R-HSA-389957 | 2.002741e-05 | 4.698 | 0 | 0 |
| AURKA Activation by TPX2 | R-HSA-8854518 | 2.097480e-05 | 4.678 | 0 | 0 |
| Cellular response to heat stress | R-HSA-3371556 | 2.209303e-05 | 4.656 | 0 | 0 |
| Formation of tubulin folding intermediates by CCT/TriC | R-HSA-389960 | 2.351794e-05 | 4.629 | 0 | 0 |
| Signaling by Nuclear Receptors | R-HSA-9006931 | 2.565525e-05 | 4.591 | 0 | 0 |
| HCMV Late Events | R-HSA-9610379 | 2.845363e-05 | 4.546 | 0 | 0 |
| Diseases of signal transduction by growth factor receptors and second messengers | R-HSA-5663202 | 2.990694e-05 | 4.524 | 1 | 0 |
| Mitochondrial unfolded protein response (UPRmt) | R-HSA-9841251 | 3.688435e-05 | 4.433 | 0 | 0 |
| Recruitment of mitotic centrosome proteins and complexes | R-HSA-380270 | 3.703494e-05 | 4.431 | 0 | 0 |
| Centrosome maturation | R-HSA-380287 | 4.313278e-05 | 4.365 | 0 | 0 |
| Programmed Cell Death | R-HSA-5357801 | 4.626398e-05 | 4.335 | 0 | 0 |
| Gene expression (Transcription) | R-HSA-74160 | 4.919709e-05 | 4.308 | 0 | 0 |
| Nuclear Envelope (NE) Reassembly | R-HSA-2995410 | 6.205239e-05 | 4.207 | 0 | 0 |
| Respiratory Syncytial Virus Infection Pathway | R-HSA-9820952 | 6.053782e-05 | 4.218 | 0 | 0 |
| SARS-CoV-2 Infection | R-HSA-9694516 | 6.718559e-05 | 4.173 | 0 | 0 |
| SARS-CoV-1-host interactions | R-HSA-9692914 | 5.652651e-05 | 4.248 | 0 | 0 |
| Regulation of actin dynamics for phagocytic cup formation | R-HSA-2029482 | 7.346398e-05 | 4.134 | 0 | 0 |
| Macroautophagy | R-HSA-1632852 | 7.346398e-05 | 4.134 | 0 | 0 |
| Sealing of the nuclear envelope (NE) by ESCRT-III | R-HSA-9668328 | 8.064498e-05 | 4.093 | 0 | 0 |
| Regulation of PLK1 Activity at G2/M Transition | R-HSA-2565942 | 8.165790e-05 | 4.088 | 0 | 0 |
| Gap junction assembly | R-HSA-190861 | 1.017437e-04 | 3.992 | 0 | 0 |
| Signaling by Interleukins | R-HSA-449147 | 1.032902e-04 | 3.986 | 1 | 0 |
| Cilium Assembly | R-HSA-5617833 | 1.221623e-04 | 3.913 | 0 | 0 |
| Epigenetic regulation of gene expression | R-HSA-212165 | 1.239750e-04 | 3.907 | 0 | 0 |
| GPVI-mediated activation cascade | R-HSA-114604 | 1.268435e-04 | 3.897 | 1 | 1 |
| Anchoring of the basal body to the plasma membrane | R-HSA-5620912 | 1.279763e-04 | 3.893 | 0 | 0 |
| Semaphorin interactions | R-HSA-373755 | 1.514257e-04 | 3.820 | 0 | 0 |
| Membrane Trafficking | R-HSA-199991 | 1.614484e-04 | 3.792 | 0 | 0 |
| Cytokine Signaling in Immune system | R-HSA-1280215 | 1.778402e-04 | 3.750 | 1 | 0 |
| Signal transduction by L1 | R-HSA-445144 | 1.853720e-04 | 3.732 | 0 | 0 |
| Attenuation phase | R-HSA-3371568 | 1.910297e-04 | 3.719 | 0 | 0 |
| Apoptosis | R-HSA-109581 | 1.935107e-04 | 3.713 | 0 | 0 |
| Activation of TRKA receptors | R-HSA-187015 | 2.006983e-04 | 3.697 | 0 | 0 |
| Assembly and cell surface presentation of NMDA receptors | R-HSA-9609736 | 2.311746e-04 | 3.636 | 0 | 0 |
| Hedgehog 'off' state | R-HSA-5610787 | 2.554711e-04 | 3.593 | 0 | 0 |
| Formation of annular gap junctions | R-HSA-196025 | 2.649846e-04 | 3.577 | 0 | 0 |
| Fcgamma receptor (FCGR) dependent phagocytosis | R-HSA-2029480 | 3.212162e-04 | 3.493 | 1 | 0 |
| Signaling by NOTCH4 | R-HSA-9013694 | 3.254984e-04 | 3.487 | 0 | 0 |
| DNA Repair | R-HSA-73894 | 3.311209e-04 | 3.480 | 0 | 0 |
| Vesicle-mediated transport | R-HSA-5653656 | 3.389507e-04 | 3.470 | 0 | 0 |
| Gap junction degradation | R-HSA-190873 | 3.412611e-04 | 3.467 | 0 | 0 |
| Carboxyterminal post-translational modifications of tubulin | R-HSA-8955332 | 3.906955e-04 | 3.408 | 0 | 0 |
| Intraflagellar transport | R-HSA-5620924 | 4.237851e-04 | 3.373 | 0 | 0 |
| PKR-mediated signaling | R-HSA-9833482 | 4.711399e-04 | 3.327 | 0 | 0 |
| HSF1-dependent transactivation | R-HSA-3371571 | 5.358127e-04 | 3.271 | 0 | 0 |
| Potential therapeutics for SARS | R-HSA-9679191 | 6.016198e-04 | 3.221 | 0 | 0 |
| Interleukin-4 and Interleukin-13 signaling | R-HSA-6785807 | 6.063971e-04 | 3.217 | 0 | 0 |
| Regulation of PTEN stability and activity | R-HSA-8948751 | 6.219730e-04 | 3.206 | 0 | 0 |
| mRNA Splicing - Major Pathway | R-HSA-72163 | 6.479996e-04 | 3.188 | 0 | 0 |
| Condensation of Prometaphase Chromosomes | R-HSA-2514853 | 6.506227e-04 | 3.187 | 0 | 0 |
| Developmental Lineage of Mammary Gland Myoepithelial Cells | R-HSA-9927432 | 6.540124e-04 | 3.184 | 0 | 0 |
| COPI-independent Golgi-to-ER retrograde traffic | R-HSA-6811436 | 7.181218e-04 | 3.144 | 0 | 0 |
| Post NMDA receptor activation events | R-HSA-438064 | 7.391000e-04 | 3.131 | 0 | 0 |
| Phosphorylation and nuclear translocation of the CRY:PER:kinase complex | R-HSA-9931530 | 7.832908e-04 | 3.106 | 0 | 0 |
| Regulation of TP53 Activity | R-HSA-5633007 | 8.714779e-04 | 3.060 | 0 | 0 |
| MHC class II antigen presentation | R-HSA-2132295 | 8.795029e-04 | 3.056 | 0 | 0 |
| mRNA Splicing | R-HSA-72172 | 9.206660e-04 | 3.036 | 0 | 0 |
| G1/S Transition | R-HSA-69206 | 9.959574e-04 | 3.002 | 0 | 0 |
| Kinesins | R-HSA-983189 | 1.006905e-03 | 2.997 | 0 | 0 |
| Sema3A PAK dependent Axon repulsion | R-HSA-399954 | 1.280435e-03 | 2.893 | 0 | 0 |
| Mitotic Anaphase | R-HSA-68882 | 1.317678e-03 | 2.880 | 0 | 0 |
| Mitotic Metaphase and Anaphase | R-HSA-2555396 | 1.356177e-03 | 2.868 | 0 | 0 |
| Cell-extracellular matrix interactions | R-HSA-446353 | 1.280435e-03 | 2.893 | 0 | 0 |
| G1/S-Specific Transcription | R-HSA-69205 | 1.392198e-03 | 2.856 | 0 | 0 |
| TRKA activation by NGF | R-HSA-187042 | 1.448385e-03 | 2.839 | 0 | 0 |
| Organelle biogenesis and maintenance | R-HSA-1852241 | 1.475437e-03 | 2.831 | 0 | 0 |
| FOXO-mediated transcription | R-HSA-9614085 | 1.475628e-03 | 2.831 | 0 | 0 |
| Prolonged ERK activation events | R-HSA-169893 | 1.481500e-03 | 2.829 | 0 | 0 |
| Hemostasis | R-HSA-109582 | 1.495124e-03 | 2.825 | 1 | 0 |
| Factors involved in megakaryocyte development and platelet production | R-HSA-983231 | 1.497875e-03 | 2.825 | 0 | 0 |
| SARS-CoV-1 Infection | R-HSA-9678108 | 1.497875e-03 | 2.825 | 0 | 0 |
| Signaling by high-kinase activity BRAF mutants | R-HSA-6802948 | 1.513413e-03 | 2.820 | 0 | 0 |
| Platelet activation, signaling and aggregation | R-HSA-76002 | 1.676466e-03 | 2.776 | 1 | 0 |
| Regulation of HSF1-mediated heat shock response | R-HSA-3371453 | 1.688264e-03 | 2.773 | 0 | 0 |
| Activation of NMDA receptors and postsynaptic events | R-HSA-442755 | 1.688264e-03 | 2.773 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G2 Cell Cycle Arrest | R-HSA-6804114 | 1.701321e-03 | 2.769 | 0 | 0 |
| Signaling by Hedgehog | R-HSA-5358351 | 1.772132e-03 | 2.752 | 0 | 0 |
| Respiratory syncytial virus (RSV) genome replication, transcription and translation | R-HSA-9820965 | 1.777549e-03 | 2.750 | 0 | 0 |
| FCGR3A-mediated phagocytosis | R-HSA-9664422 | 1.903671e-03 | 2.720 | 1 | 1 |
| Leishmania phagocytosis | R-HSA-9664417 | 1.903671e-03 | 2.720 | 1 | 0 |
| Parasite infection | R-HSA-9664407 | 1.903671e-03 | 2.720 | 1 | 0 |
| Cargo trafficking to the periciliary membrane | R-HSA-5620920 | 1.935297e-03 | 2.713 | 0 | 0 |
| Transcriptional and post-translational regulation of MITF-M expression and activity | R-HSA-9856649 | 1.935297e-03 | 2.713 | 0 | 0 |
| SPOP-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929491 | 2.072067e-03 | 2.684 | 0 | 0 |
| Signaling by ALK fusions and activated point mutants | R-HSA-9725370 | 2.182574e-03 | 2.661 | 0 | 0 |
| Signaling by ALK in cancer | R-HSA-9700206 | 2.182574e-03 | 2.661 | 0 | 0 |
| Chaperone Mediated Autophagy | R-HSA-9613829 | 2.199635e-03 | 2.658 | 0 | 0 |
| Signaling by RAF1 mutants | R-HSA-9656223 | 2.231256e-03 | 2.651 | 0 | 0 |
| MAP2K and MAPK activation | R-HSA-5674135 | 2.231256e-03 | 2.651 | 0 | 0 |
| Interleukin-3, Interleukin-5 and GM-CSF signaling | R-HSA-512988 | 2.398682e-03 | 2.620 | 1 | 0 |
| Mitotic G1 phase and G1/S transition | R-HSA-453279 | 2.424596e-03 | 2.615 | 1 | 0 |
| Interleukin-12 signaling | R-HSA-9020591 | 2.517862e-03 | 2.599 | 0 | 0 |
| PIP3 activates AKT signaling | R-HSA-1257604 | 2.749138e-03 | 2.561 | 0 | 0 |
| Phosphorylation and nuclear translocation of BMAL1 (ARNTL) and CLOCK | R-HSA-9931529 | 2.798205e-03 | 2.553 | 0 | 0 |
| KEAP1-NFE2L2 pathway | R-HSA-9755511 | 2.859365e-03 | 2.544 | 0 | 0 |
| NOTCH4 Intracellular Domain Regulates Transcription | R-HSA-9013695 | 3.102122e-03 | 2.508 | 0 | 0 |
| Antiviral mechanism by IFN-stimulated genes | R-HSA-1169410 | 3.147508e-03 | 2.502 | 0 | 0 |
| Signaling downstream of RAS mutants | R-HSA-9649948 | 3.154936e-03 | 2.501 | 0 | 0 |
| Paradoxical activation of RAF signaling by kinase inactive BRAF | R-HSA-6802955 | 3.154936e-03 | 2.501 | 0 | 0 |
| Signaling by moderate kinase activity BRAF mutants | R-HSA-6802946 | 3.154936e-03 | 2.501 | 0 | 0 |
| Signaling by RAS mutants | R-HSA-6802949 | 3.154936e-03 | 2.501 | 0 | 0 |
| Nuclear events stimulated by ALK signaling in cancer | R-HSA-9725371 | 3.587871e-03 | 2.445 | 0 | 0 |
| NGF-independant TRKA activation | R-HSA-187024 | 3.628586e-03 | 2.440 | 0 | 0 |
| Resolution of Sister Chromatid Cohesion | R-HSA-2500257 | 4.033969e-03 | 2.394 | 0 | 0 |
| Regulation of PD-L1(CD274) Post-translational modification | R-HSA-9909615 | 4.049427e-03 | 2.393 | 0 | 0 |
| Regulation of TP53 Activity through Phosphorylation | R-HSA-6804756 | 4.232427e-03 | 2.373 | 0 | 0 |
| Separation of Sister Chromatids | R-HSA-2467813 | 4.270605e-03 | 2.370 | 0 | 0 |
| Interleukin-12 family signaling | R-HSA-447115 | 4.421258e-03 | 2.354 | 0 | 0 |
| MITF-M-regulated melanocyte development | R-HSA-9730414 | 4.537243e-03 | 2.343 | 0 | 0 |
| TFAP2A acts as a transcriptional repressor during retinoic acid induced cell differentiation | R-HSA-8869496 | 4.559520e-03 | 2.341 | 0 | 0 |
| Smooth Muscle Contraction | R-HSA-445355 | 4.842839e-03 | 2.315 | 0 | 0 |
| Signaling by NTRK1 (TRKA) | R-HSA-187037 | 5.306887e-03 | 2.275 | 0 | 0 |
| Activated NTRK2 signals through CDK5 | R-HSA-9032845 | 5.588735e-03 | 2.253 | 0 | 0 |
| SHOC2 M1731 mutant abolishes MRAS complex function | R-HSA-9726840 | 5.588735e-03 | 2.253 | 0 | 0 |
| Uptake and function of diphtheria toxin | R-HSA-5336415 | 5.588735e-03 | 2.253 | 0 | 0 |
| Negative regulation of the PI3K/AKT network | R-HSA-199418 | 5.666471e-03 | 2.247 | 0 | 0 |
| Extracellular matrix organization | R-HSA-1474244 | 5.808334e-03 | 2.236 | 0 | 0 |
| Antigen activates B Cell Receptor (BCR) leading to generation of second messengers | R-HSA-983695 | 5.914677e-03 | 2.228 | 1 | 1 |
| TP53 Regulates Transcription of Cell Cycle Genes | R-HSA-6791312 | 6.036909e-03 | 2.219 | 0 | 0 |
| Processing of Capped Intron-Containing Pre-mRNA | R-HSA-72203 | 6.195637e-03 | 2.208 | 0 | 0 |
| Signaling by MRAS-complex mutants | R-HSA-9660537 | 6.713996e-03 | 2.173 | 0 | 0 |
| Gain-of-function MRAS complexes activate RAF signaling | R-HSA-9726842 | 6.713996e-03 | 2.173 | 0 | 0 |
| Interleukin-18 signaling | R-HSA-9012546 | 6.713996e-03 | 2.173 | 0 | 0 |
| ARMS-mediated activation | R-HSA-170984 | 7.933103e-03 | 2.101 | 0 | 0 |
| Signaling by BRAF and RAF1 fusions | R-HSA-6802952 | 8.980033e-03 | 2.047 | 0 | 0 |
| DAP12 signaling | R-HSA-2424491 | 7.603350e-03 | 2.119 | 0 | 0 |
| MAPK3 (ERK1) activation | R-HSA-110056 | 9.243895e-03 | 2.034 | 0 | 0 |
| Regulation of APC/C activators between G1/S and early anaphase | R-HSA-176408 | 7.785905e-03 | 2.109 | 0 | 0 |
| WNT mediated activation of DVL | R-HSA-201688 | 7.933103e-03 | 2.101 | 0 | 0 |
| Assembly and release of respiratory syncytial virus (RSV) virions | R-HSA-9820962 | 9.243895e-03 | 2.034 | 0 | 0 |
| Intracellular signaling by second messengers | R-HSA-9006925 | 7.141851e-03 | 2.146 | 0 | 0 |
| G0 and Early G1 | R-HSA-1538133 | 8.801207e-03 | 2.055 | 0 | 0 |
| Respiratory syncytial virus genome replication | R-HSA-9834752 | 7.933103e-03 | 2.101 | 0 | 0 |
| COPI-dependent Golgi-to-ER retrograde traffic | R-HSA-6811434 | 6.911535e-03 | 2.160 | 0 | 0 |
| Formation of paraxial mesoderm | R-HSA-9793380 | 7.412411e-03 | 2.130 | 0 | 0 |
| COPI-mediated anterograde transport | R-HSA-6807878 | 6.911535e-03 | 2.160 | 0 | 0 |
| Receptor Mediated Mitophagy | R-HSA-8934903 | 9.243895e-03 | 2.034 | 0 | 0 |
| Regulation of CDH1 posttranslational processing and trafficking to plasma membrane | R-HSA-9768727 | 1.010353e-02 | 1.996 | 0 | 0 |
| Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation | R-HSA-8950505 | 8.980033e-03 | 2.047 | 0 | 0 |
| Signaling by NTRKs | R-HSA-166520 | 1.058998e-02 | 1.975 | 0 | 0 |
| ChREBP activates metabolic gene expression | R-HSA-163765 | 1.064424e-02 | 1.973 | 0 | 0 |
| Drug resistance of PDGFR mutants | R-HSA-9674415 | 1.093189e-02 | 1.961 | 0 | 0 |
| PDGFR mutants bind TKIs | R-HSA-9674428 | 1.093189e-02 | 1.961 | 0 | 0 |
| Regorafenib-resistant PDGFR mutants | R-HSA-9674403 | 1.093189e-02 | 1.961 | 0 | 0 |
| Imatinib-resistant PDGFR mutants | R-HSA-9674396 | 1.093189e-02 | 1.961 | 0 | 0 |
| Sorafenib-resistant PDGFR mutants | R-HSA-9674404 | 1.093189e-02 | 1.961 | 0 | 0 |
| Sunitinib-resistant PDGFR mutants | R-HSA-9674401 | 1.093189e-02 | 1.961 | 0 | 0 |
| EML4 and NUDC in mitotic spindle formation | R-HSA-9648025 | 1.132136e-02 | 1.946 | 0 | 0 |
| Signalling to ERKs | R-HSA-187687 | 1.151198e-02 | 1.939 | 0 | 0 |
| APC/C-mediated degradation of cell cycle proteins | R-HSA-174143 | 1.171307e-02 | 1.931 | 0 | 0 |
| Regulation of mitotic cell cycle | R-HSA-453276 | 1.171307e-02 | 1.931 | 0 | 0 |
| NFE2L2 regulates pentose phosphate pathway genes | R-HSA-9818028 | 1.213206e-02 | 1.916 | 0 | 0 |
| Developmental Lineages of the Mammary Gland | R-HSA-9924644 | 1.221490e-02 | 1.913 | 0 | 0 |
| Regulation of mRNA stability by proteins that bind AU-rich elements | R-HSA-450531 | 1.221490e-02 | 1.913 | 0 | 0 |
| Regulation of TP53 Degradation | R-HSA-6804757 | 1.225645e-02 | 1.912 | 0 | 0 |
| Cell death signalling via NRAGE, NRIF and NADE | R-HSA-204998 | 1.273030e-02 | 1.895 | 0 | 0 |
| Scavenging by Class F Receptors | R-HSA-3000484 | 1.370528e-02 | 1.863 | 0 | 0 |
| Signaling by the B Cell Receptor (BCR) | R-HSA-983705 | 1.377033e-02 | 1.861 | 1 | 0 |
| Metabolism of RNA | R-HSA-8953854 | 1.379382e-02 | 1.860 | 0 | 0 |
| Regulation of TP53 Expression and Degradation | R-HSA-6806003 | 1.465265e-02 | 1.834 | 0 | 0 |
| Cellular response to chemical stress | R-HSA-9711123 | 1.498318e-02 | 1.824 | 0 | 0 |
| Frs2-mediated activation | R-HSA-170968 | 1.536189e-02 | 1.814 | 0 | 0 |
| Negative regulation of NOTCH4 signaling | R-HSA-9604323 | 1.550606e-02 | 1.809 | 0 | 0 |
| PI3K/AKT Signaling in Cancer | R-HSA-2219528 | 1.590706e-02 | 1.798 | 0 | 0 |
| Retrograde neurotrophin signalling | R-HSA-177504 | 1.709989e-02 | 1.767 | 0 | 0 |
| CRMPs in Sema3A signaling | R-HSA-399956 | 1.709989e-02 | 1.767 | 0 | 0 |
| MTOR signalling | R-HSA-165159 | 1.823157e-02 | 1.739 | 0 | 0 |
| PI5P, PP2A and IER3 Regulate PI3K/AKT Signaling | R-HSA-6811558 | 1.834912e-02 | 1.736 | 0 | 0 |
| Butyrate Response Factor 1 (BRF1) binds and destabilizes mRNA | R-HSA-450385 | 1.891733e-02 | 1.723 | 0 | 0 |
| Parasitic Infection Pathways | R-HSA-9824443 | 1.895964e-02 | 1.722 | 1 | 0 |
| Leishmania infection | R-HSA-9658195 | 1.895964e-02 | 1.722 | 1 | 0 |
| Signaling by SCF-KIT | R-HSA-1433557 | 1.919540e-02 | 1.717 | 1 | 1 |
| Oncogenic MAPK signaling | R-HSA-6802957 | 2.001544e-02 | 1.699 | 0 | 0 |
| DAP12 interactions | R-HSA-2172127 | 2.018698e-02 | 1.695 | 0 | 0 |
| Phosphorylation of the APC/C | R-HSA-176412 | 2.081228e-02 | 1.682 | 0 | 0 |
| KSRP (KHSRP) binds and destabilizes mRNA | R-HSA-450604 | 2.081228e-02 | 1.682 | 0 | 0 |
| Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 | R-HSA-1362300 | 2.081228e-02 | 1.682 | 0 | 0 |
| MAPK family signaling cascades | R-HSA-5683057 | 2.100270e-02 | 1.678 | 0 | 0 |
| Somitogenesis | R-HSA-9824272 | 2.120632e-02 | 1.674 | 0 | 0 |
| MAPK1/MAPK3 signaling | R-HSA-5684996 | 2.442747e-02 | 1.612 | 0 | 0 |
| Co-stimulation by CD28 | R-HSA-389356 | 2.443109e-02 | 1.612 | 1 | 1 |
| Golgi-to-ER retrograde transport | R-HSA-8856688 | 2.456177e-02 | 1.610 | 0 | 0 |
| Signaling by Hippo | R-HSA-2028269 | 2.482720e-02 | 1.605 | 0 | 0 |
| Azathioprine ADME | R-HSA-9748787 | 2.671980e-02 | 1.573 | 0 | 0 |
| Eukaryotic Translation Elongation | R-HSA-156842 | 2.687626e-02 | 1.571 | 0 | 0 |
| Depolymerization of the Nuclear Lamina | R-HSA-4419969 | 2.694347e-02 | 1.570 | 0 | 0 |
| Cdc20:Phospho-APC/C mediated degradation of Cyclin A | R-HSA-174184 | 2.911932e-02 | 1.536 | 0 | 0 |
| Uptake and actions of bacterial toxins | R-HSA-5339562 | 2.911932e-02 | 1.536 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Cyclin B | R-HSA-174048 | 2.912988e-02 | 1.536 | 0 | 0 |
| Regulation of signaling by CBL | R-HSA-912631 | 2.912988e-02 | 1.536 | 1 | 1 |
| Mechanical load activates signaling by PIEZO1 and integrins in osteocytes | R-HSA-9856532 | 2.912988e-02 | 1.536 | 0 | 0 |
| Rap1 signalling | R-HSA-392517 | 2.912988e-02 | 1.536 | 0 | 0 |
| PTEN Regulation | R-HSA-6807070 | 2.983977e-02 | 1.525 | 0 | 0 |
| APC:Cdc20 mediated degradation of cell cycle proteins prior to satisfation of the cell cycle checkpoint | R-HSA-179419 | 3.036051e-02 | 1.518 | 0 | 0 |
| Co-inhibition by CTLA4 | R-HSA-389513 | 3.138466e-02 | 1.503 | 1 | 1 |
| CDK-mediated phosphorylation and removal of Cdc6 | R-HSA-69017 | 3.162923e-02 | 1.500 | 0 | 0 |
| Manipulation of host energy metabolism | R-HSA-9636667 | 3.244044e-02 | 1.489 | 0 | 0 |
| SARS-CoV-2 activates/modulates innate and adaptive immune responses | R-HSA-9705671 | 3.272730e-02 | 1.485 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176409 | 3.292541e-02 | 1.482 | 0 | 0 |
| p75 NTR receptor-mediated signalling | R-HSA-193704 | 3.402352e-02 | 1.468 | 0 | 0 |
| Activation of APC/C and APC/C:Cdc20 mediated degradation of mitotic proteins | R-HSA-176814 | 3.424896e-02 | 1.465 | 0 | 0 |
| NRAGE signals death through JNK | R-HSA-193648 | 3.424896e-02 | 1.465 | 0 | 0 |
| Interferon Signaling | R-HSA-913531 | 3.558853e-02 | 1.449 | 0 | 0 |
| Inactivation of CSF3 (G-CSF) signaling | R-HSA-9705462 | 3.609239e-02 | 1.443 | 1 | 1 |
| Initiation of Nuclear Envelope (NE) Reformation | R-HSA-2995383 | 3.609239e-02 | 1.443 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in cell cycle and proliferation | R-HSA-9825892 | 3.609239e-02 | 1.443 | 0 | 0 |
| ER to Golgi Anterograde Transport | R-HSA-199977 | 3.657446e-02 | 1.437 | 0 | 0 |
| Developmental Lineage of Mammary Stem Cells | R-HSA-9938206 | 3.854196e-02 | 1.414 | 0 | 0 |
| Regulation of IFNA/IFNB signaling | R-HSA-912694 | 3.854196e-02 | 1.414 | 0 | 0 |
| RAF-independent MAPK1/3 activation | R-HSA-112409 | 3.854196e-02 | 1.414 | 0 | 0 |
| RSV-host interactions | R-HSA-9833110 | 4.004354e-02 | 1.397 | 0 | 0 |
| Interleukin-1 family signaling | R-HSA-446652 | 4.068925e-02 | 1.391 | 0 | 0 |
| Constitutive Signaling by AKT1 E17K in Cancer | R-HSA-5674400 | 4.105312e-02 | 1.387 | 0 | 0 |
| Syndecan interactions | R-HSA-3000170 | 4.105312e-02 | 1.387 | 0 | 0 |
| G beta:gamma signalling through PI3Kgamma | R-HSA-392451 | 4.105312e-02 | 1.387 | 0 | 0 |
| Drug resistance in ERBB2 KD mutants | R-HSA-9665230 | 4.301965e-02 | 1.366 | 0 | 0 |
| BDNF activates NTRK2 (TRKB) signaling | R-HSA-9024909 | 4.301965e-02 | 1.366 | 0 | 0 |
| Drug-mediated inhibition of ERBB2 signaling | R-HSA-9652282 | 4.301965e-02 | 1.366 | 0 | 0 |
| NTF4 activates NTRK2 (TRKB) signaling | R-HSA-9026357 | 4.301965e-02 | 1.366 | 0 | 0 |
| NTF3 activates NTRK2 (TRKB) signaling | R-HSA-9025046 | 4.301965e-02 | 1.366 | 0 | 0 |
| Resistance of ERBB2 KD mutants to afatinib | R-HSA-9665249 | 4.301965e-02 | 1.366 | 0 | 0 |
| Resistance of ERBB2 KD mutants to AEE788 | R-HSA-9665250 | 4.301965e-02 | 1.366 | 0 | 0 |
| Resistance of ERBB2 KD mutants to lapatinib | R-HSA-9665251 | 4.301965e-02 | 1.366 | 0 | 0 |
| Defective AHCY causes HMAHCHD | R-HSA-5578997 | 4.301965e-02 | 1.366 | 0 | 0 |
| Resistance of ERBB2 KD mutants to osimertinib | R-HSA-9665247 | 4.301965e-02 | 1.366 | 0 | 0 |
| Drug resistance in ERBB2 TMD/JMD mutants | R-HSA-9665737 | 4.301965e-02 | 1.366 | 0 | 0 |
| Resistance of ERBB2 KD mutants to tesevatinib | R-HSA-9665245 | 4.301965e-02 | 1.366 | 0 | 0 |
| Resistance of ERBB2 KD mutants to sapitinib | R-HSA-9665244 | 4.301965e-02 | 1.366 | 0 | 0 |
| Resistance of ERBB2 KD mutants to trastuzumab | R-HSA-9665233 | 4.301965e-02 | 1.366 | 0 | 0 |
| Resistance of ERBB2 KD mutants to neratinib | R-HSA-9665246 | 4.301965e-02 | 1.366 | 0 | 0 |
| PLC-gamma1 signalling | R-HSA-167021 | 5.348384e-02 | 1.272 | 0 | 0 |
| Signalling to STAT3 | R-HSA-198745 | 5.348384e-02 | 1.272 | 0 | 0 |
| Activated NTRK2 signals through PLCG1 | R-HSA-9026527 | 6.383425e-02 | 1.195 | 0 | 0 |
| Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 complexes | R-HSA-69200 | 6.383425e-02 | 1.195 | 0 | 0 |
| IRS activation | R-HSA-74713 | 7.407210e-02 | 1.130 | 0 | 0 |
| NTRK2 activates RAC1 | R-HSA-9032759 | 7.407210e-02 | 1.130 | 0 | 0 |
| G2 Phase | R-HSA-68911 | 7.407210e-02 | 1.130 | 0 | 0 |
| Signalling to p38 via RIT and RIN | R-HSA-187706 | 8.419862e-02 | 1.075 | 0 | 0 |
| CDH11 homotypic and heterotypic interactions | R-HSA-9833576 | 8.419862e-02 | 1.075 | 0 | 0 |
| PTK6 Regulates Cell Cycle | R-HSA-8849470 | 8.419862e-02 | 1.075 | 0 | 0 |
| Translocation of ZAP-70 to Immunological synapse | R-HSA-202430 | 4.362425e-02 | 1.360 | 0 | 0 |
| Signaling by NTRK2 (TRKB) | R-HSA-9006115 | 5.168164e-02 | 1.287 | 0 | 0 |
| Striated Muscle Contraction | R-HSA-390522 | 7.229616e-02 | 1.141 | 0 | 0 |
| RAF activation | R-HSA-5673000 | 7.542750e-02 | 1.122 | 0 | 0 |
| Cyclin A/B1/B2 associated events during G2/M transition | R-HSA-69273 | 6.920868e-02 | 1.160 | 0 | 0 |
| Cyclin A:Cdk2-associated events at S phase entry | R-HSA-69656 | 5.904954e-02 | 1.229 | 0 | 0 |
| CD22 mediated BCR regulation | R-HSA-5690714 | 4.581000e-02 | 1.339 | 1 | 1 |
| Cyclin E associated events during G1/S transition | R-HSA-69202 | 5.558688e-02 | 1.255 | 0 | 0 |
| Aberrant regulation of mitotic cell cycle due to RB1 defects | R-HSA-9687139 | 6.022294e-02 | 1.220 | 0 | 0 |
| Aryl hydrocarbon receptor signalling | R-HSA-8937144 | 8.419862e-02 | 1.075 | 0 | 0 |
| Neurodegenerative Diseases | R-HSA-8863678 | 4.362425e-02 | 1.360 | 0 | 0 |
| Deregulated CDK5 triggers multiple neurodegenerative pathways in Alzheimer's disease models | R-HSA-8862803 | 4.362425e-02 | 1.360 | 0 | 0 |
| CD28 dependent PI3K/Akt signaling | R-HSA-389357 | 5.168164e-02 | 1.287 | 0 | 0 |
| Defective Intrinsic Pathway for Apoptosis | R-HSA-9734009 | 5.168164e-02 | 1.287 | 0 | 0 |
| Signaling by CSF3 (G-CSF) | R-HSA-9674555 | 5.732455e-02 | 1.242 | 1 | 1 |
| Localization of the PINCH-ILK-PARVIN complex to focal adhesions | R-HSA-446343 | 4.301965e-02 | 1.366 | 0 | 0 |
| MET interacts with TNS proteins | R-HSA-8875513 | 5.348384e-02 | 1.272 | 0 | 0 |
| AKT-mediated inactivation of FOXO1A | R-HSA-211163 | 6.383425e-02 | 1.195 | 0 | 0 |
| Phosphorylation of Emi1 | R-HSA-176417 | 8.419862e-02 | 1.075 | 0 | 0 |
| Interaction between L1 and Ankyrins | R-HSA-445095 | 5.168164e-02 | 1.287 | 0 | 0 |
| Lysosome Vesicle Biogenesis | R-HSA-432720 | 8.181655e-02 | 1.087 | 0 | 0 |
| Switching of origins to a post-replicative state | R-HSA-69052 | 6.081823e-02 | 1.216 | 0 | 0 |
| Developmental Cell Lineages of the Integumentary System | R-HSA-9734779 | 4.437278e-02 | 1.353 | 0 | 0 |
| FCERI mediated Ca+2 mobilization | R-HSA-2871809 | 5.503562e-02 | 1.259 | 1 | 1 |
| eNOS activation | R-HSA-203615 | 7.542750e-02 | 1.122 | 0 | 0 |
| Diseases of mitotic cell cycle | R-HSA-9675126 | 6.616641e-02 | 1.179 | 0 | 0 |
| FCERI mediated MAPK activation | R-HSA-2871796 | 4.895461e-02 | 1.310 | 1 | 1 |
| NADE modulates death signalling | R-HSA-205025 | 6.383425e-02 | 1.195 | 0 | 0 |
| Biosynthesis of DPAn-3-derived 13-series resolvins | R-HSA-9026403 | 7.407210e-02 | 1.130 | 0 | 0 |
| Respiratory syncytial virus (RSV) attachment and entry | R-HSA-9820960 | 6.317070e-02 | 1.199 | 0 | 0 |
| FLT3 signaling through SRC family kinases | R-HSA-9706374 | 6.383425e-02 | 1.195 | 0 | 0 |
| Co-inhibition by BTLA | R-HSA-9927353 | 7.407210e-02 | 1.130 | 0 | 0 |
| Downregulation of ERBB2 signaling | R-HSA-8863795 | 6.022294e-02 | 1.220 | 0 | 0 |
| Regulation of CDH19 Expression and Function | R-HSA-9764302 | 8.419862e-02 | 1.075 | 0 | 0 |
| RUNX1 interacts with co-factors whose precise effect on RUNX1 targets is not known | R-HSA-8939243 | 6.920868e-02 | 1.160 | 0 | 0 |
| Muscle contraction | R-HSA-397014 | 4.420582e-02 | 1.355 | 0 | 0 |
| Regulation of necroptotic cell death | R-HSA-5675482 | 6.920868e-02 | 1.160 | 0 | 0 |
| Nectin/Necl trans heterodimerization | R-HSA-420597 | 7.407210e-02 | 1.130 | 0 | 0 |
| Tetrahydrobiopterin (BH4) synthesis, recycling, salvage and regulation | R-HSA-1474151 | 6.022294e-02 | 1.220 | 0 | 0 |
| Integrin signaling | R-HSA-354192 | 6.920868e-02 | 1.160 | 0 | 0 |
| Metabolism of proteins | R-HSA-392499 | 8.011927e-02 | 1.096 | 0 | 0 |
| MAPK6/MAPK4 signaling | R-HSA-5687128 | 8.390222e-02 | 1.076 | 0 | 0 |
| Cooperation of PDCL (PhLP1) and TRiC/CCT in G-protein beta folding | R-HSA-6814122 | 7.542750e-02 | 1.122 | 0 | 0 |
| Circadian clock | R-HSA-9909396 | 8.165102e-02 | 1.088 | 0 | 0 |
| NPAS4 regulates expression of target genes | R-HSA-9768919 | 7.542750e-02 | 1.122 | 0 | 0 |
| Interleukin-37 signaling | R-HSA-9008059 | 6.022294e-02 | 1.220 | 0 | 0 |
| G-protein beta:gamma signalling | R-HSA-397795 | 6.920868e-02 | 1.160 | 0 | 0 |
| G alpha (12/13) signalling events | R-HSA-416482 | 7.002697e-02 | 1.155 | 0 | 0 |
| Maturation of hRSV A proteins | R-HSA-9828806 | 5.168164e-02 | 1.287 | 0 | 0 |
| Nuclear events mediated by NFE2L2 | R-HSA-9759194 | 6.284699e-02 | 1.202 | 0 | 0 |
| Neurotransmitter receptors and postsynaptic signal transmission | R-HSA-112314 | 4.420582e-02 | 1.355 | 0 | 0 |
| Mitophagy | R-HSA-5205647 | 7.542750e-02 | 1.122 | 0 | 0 |
| Deactivation of the beta-catenin transactivating complex | R-HSA-3769402 | 8.507168e-02 | 1.070 | 0 | 0 |
| Metabolism of nitric oxide: NOS3 activation and regulation | R-HSA-202131 | 8.836556e-02 | 1.054 | 0 | 0 |
| RIPK1-mediated regulated necrosis | R-HSA-5213460 | 8.836556e-02 | 1.054 | 0 | 0 |
| Transcriptional Regulation by E2F6 | R-HSA-8953750 | 9.169696e-02 | 1.038 | 0 | 0 |
| G2/M DNA replication checkpoint | R-HSA-69478 | 9.421501e-02 | 1.026 | 0 | 0 |
| E2F-enabled inhibition of pre-replication complex formation | R-HSA-113507 | 9.421501e-02 | 1.026 | 0 | 0 |
| Activation of NIMA Kinases NEK9, NEK6, NEK7 | R-HSA-2980767 | 9.421501e-02 | 1.026 | 0 | 0 |
| Nef and signal transduction | R-HSA-164944 | 9.421501e-02 | 1.026 | 0 | 0 |
| Generation of second messenger molecules | R-HSA-202433 | 9.506467e-02 | 1.022 | 0 | 0 |
| Interleukin-2 family signaling | R-HSA-451927 | 9.506467e-02 | 1.022 | 0 | 0 |
| Intra-Golgi and retrograde Golgi-to-ER traffic | R-HSA-6811442 | 9.539438e-02 | 1.020 | 0 | 0 |
| Transport to the Golgi and subsequent modification | R-HSA-948021 | 9.817103e-02 | 1.008 | 0 | 0 |
| FLT3 Signaling | R-HSA-9607240 | 9.846751e-02 | 1.007 | 0 | 0 |
| Fc epsilon receptor (FCERI) signaling | R-HSA-2454202 | 9.957462e-02 | 1.002 | 1 | 1 |
| Negative regulation of MAPK pathway | R-HSA-5675221 | 1.019043e-01 | 0.992 | 0 | 0 |
| Clathrin-mediated endocytosis | R-HSA-8856828 | 1.029089e-01 | 0.988 | 0 | 0 |
| CHL1 interactions | R-HSA-447041 | 1.041225e-01 | 0.982 | 0 | 0 |
| Developmental Lineage of Mammary Gland Luminal Epithelial Cells | R-HSA-9927418 | 1.053740e-01 | 0.977 | 0 | 0 |
| Constitutive Signaling by Aberrant PI3K in Cancer | R-HSA-2219530 | 1.078423e-01 | 0.967 | 0 | 0 |
| Post-translational protein modification | R-HSA-597592 | 1.104573e-01 | 0.957 | 0 | 0 |
| S Phase | R-HSA-69242 | 1.116999e-01 | 0.952 | 0 | 0 |
| SCF(Skp2)-mediated degradation of p27/p21 | R-HSA-187577 | 1.124073e-01 | 0.949 | 0 | 0 |
| Proteasome assembly | R-HSA-9907900 | 1.124073e-01 | 0.949 | 0 | 0 |
| Transcriptional regulation by the AP-2 (TFAP2) family of transcription factors | R-HSA-8864260 | 1.124073e-01 | 0.949 | 0 | 0 |
| EPHB-mediated forward signaling | R-HSA-3928662 | 1.124073e-01 | 0.949 | 1 | 1 |
| Gastrulation | R-HSA-9758941 | 1.134973e-01 | 0.945 | 0 | 0 |
| Activated NTRK2 signals through FYN | R-HSA-9032500 | 1.139221e-01 | 0.943 | 0 | 0 |
| Activated NTRK2 signals through PI3K | R-HSA-9028335 | 1.139221e-01 | 0.943 | 0 | 0 |
| Interleukin-23 signaling | R-HSA-9020933 | 1.139221e-01 | 0.943 | 0 | 0 |
| PTK6 Regulates RTKs and Their Effectors AKT1 and DOK1 | R-HSA-8849469 | 1.139221e-01 | 0.943 | 0 | 0 |
| Platelet Aggregation (Plug Formation) | R-HSA-76009 | 1.159689e-01 | 0.936 | 0 | 0 |
| Autodegradation of Cdh1 by Cdh1:APC/C | R-HSA-174084 | 1.195589e-01 | 0.922 | 0 | 0 |
| Death Receptor Signaling | R-HSA-73887 | 1.226744e-01 | 0.911 | 0 | 0 |
| APC/C:Cdc20 mediated degradation of Securin | R-HSA-174154 | 1.231763e-01 | 0.909 | 0 | 0 |
| Synthesis of PC | R-HSA-1483191 | 1.231763e-01 | 0.909 | 0 | 0 |
| AKT phosphorylates targets in the nucleus | R-HSA-198693 | 1.236152e-01 | 0.908 | 0 | 0 |
| ALK mutants bind TKIs | R-HSA-9700645 | 1.236152e-01 | 0.908 | 0 | 0 |
| AMPK inhibits chREBP transcriptional activation activity | R-HSA-163680 | 1.236152e-01 | 0.908 | 0 | 0 |
| Lipophagy | R-HSA-9613354 | 1.236152e-01 | 0.908 | 0 | 0 |
| GP1b-IX-V activation signalling | R-HSA-430116 | 1.236152e-01 | 0.908 | 0 | 0 |
| MAPK1 (ERK2) activation | R-HSA-112411 | 1.236152e-01 | 0.908 | 0 | 0 |
| MASTL Facilitates Mitotic Progression | R-HSA-2465910 | 1.236152e-01 | 0.908 | 0 | 0 |
| NOTCH4 Activation and Transmission of Signal to the Nucleus | R-HSA-9013700 | 1.236152e-01 | 0.908 | 0 | 0 |
| Extra-nuclear estrogen signaling | R-HSA-9009391 | 1.267247e-01 | 0.897 | 0 | 0 |
| Gluconeogenesis | R-HSA-70263 | 1.268202e-01 | 0.897 | 0 | 0 |
| RAF/MAP kinase cascade | R-HSA-5673001 | 1.270399e-01 | 0.896 | 0 | 0 |
| Degradation of CDH1 | R-HSA-9766229 | 1.304895e-01 | 0.884 | 0 | 0 |
| p53-Dependent G1/S DNA damage checkpoint | R-HSA-69580 | 1.304895e-01 | 0.884 | 0 | 0 |
| p53-Dependent G1 DNA Damage Response | R-HSA-69563 | 1.304895e-01 | 0.884 | 0 | 0 |
| Folding of actin by CCT/TriC | R-HSA-390450 | 1.332029e-01 | 0.875 | 0 | 0 |
| Regulation of CDH11 function | R-HSA-9762292 | 1.332029e-01 | 0.875 | 0 | 0 |
| PI3K/AKT activation | R-HSA-198203 | 1.332029e-01 | 0.875 | 0 | 0 |
| WNT5A-dependent internalization of FZD2, FZD5 and ROR2 | R-HSA-5140745 | 1.332029e-01 | 0.875 | 0 | 0 |
| Activation of PPARGC1A (PGC-1alpha) by phosphorylation | R-HSA-2151209 | 1.332029e-01 | 0.875 | 0 | 0 |
| Interleukin-27 signaling | R-HSA-9020956 | 1.332029e-01 | 0.875 | 0 | 0 |
| Insulin-like Growth Factor-2 mRNA Binding Proteins (IGF2BPs/IMPs/VICKZs) bind RNA | R-HSA-428359 | 1.332029e-01 | 0.875 | 0 | 0 |
| Signal attenuation | R-HSA-74749 | 1.332029e-01 | 0.875 | 0 | 0 |
| mRNA 3'-end processing | R-HSA-72187 | 1.416402e-01 | 0.849 | 0 | 0 |
| Orc1 removal from chromatin | R-HSA-68949 | 1.416402e-01 | 0.849 | 0 | 0 |
| AMPK-induced ERAD and lysosome mediated degradation of PD-L1(CD274) | R-HSA-9931269 | 1.416402e-01 | 0.849 | 0 | 0 |
| Transcriptional Regulation by NPAS4 | R-HSA-9634815 | 1.416402e-01 | 0.849 | 0 | 0 |
| InlA-mediated entry of Listeria monocytogenes into host cells | R-HSA-8876493 | 1.426862e-01 | 0.846 | 0 | 0 |
| vRNP Assembly | R-HSA-192905 | 1.426862e-01 | 0.846 | 0 | 0 |
| Biosynthesis of DPAn-3-derived maresins | R-HSA-9026290 | 1.426862e-01 | 0.846 | 0 | 0 |
| PECAM1 interactions | R-HSA-210990 | 1.426862e-01 | 0.846 | 1 | 1 |
| RUNX2 regulates genes involved in cell migration | R-HSA-8941332 | 1.426862e-01 | 0.846 | 0 | 0 |
| Interleukin-2 signaling | R-HSA-9020558 | 1.426862e-01 | 0.846 | 0 | 0 |
| Synthesis of DNA | R-HSA-69239 | 1.441417e-01 | 0.841 | 0 | 0 |
| APC/C:Cdh1 mediated degradation of Cdc20 and other APC/C:Cdh1 targeted proteins in late mitosis/early G1 | R-HSA-174178 | 1.454016e-01 | 0.837 | 0 | 0 |
| TCR signaling | R-HSA-202403 | 1.518374e-01 | 0.819 | 0 | 0 |
| Activated NTRK2 signals through RAS | R-HSA-9026519 | 1.520664e-01 | 0.818 | 0 | 0 |
| Sensory processing of sound by outer hair cells of the cochlea | R-HSA-9662361 | 1.568062e-01 | 0.805 | 0 | 0 |
| Nuclear Envelope Breakdown | R-HSA-2980766 | 1.606450e-01 | 0.794 | 0 | 0 |
| AKT phosphorylates targets in the cytosol | R-HSA-198323 | 1.613445e-01 | 0.792 | 0 | 0 |
| Activated NTRK2 signals through FRS2 and FRS3 | R-HSA-9028731 | 1.613445e-01 | 0.792 | 0 | 0 |
| Defective EXT2 causes exostoses 2 | R-HSA-3656237 | 1.613445e-01 | 0.792 | 0 | 0 |
| Defective EXT1 causes exostoses 1, TRPS2 and CHDS | R-HSA-3656253 | 1.613445e-01 | 0.792 | 0 | 0 |
| RUNX3 regulates NOTCH signaling | R-HSA-8941856 | 1.613445e-01 | 0.792 | 0 | 0 |
| SHC-related events triggered by IGF1R | R-HSA-2428933 | 1.613445e-01 | 0.792 | 0 | 0 |
| Constitutive Signaling by Overexpressed ERBB2 | R-HSA-9634285 | 1.613445e-01 | 0.792 | 0 | 0 |
| VLDLR internalisation and degradation | R-HSA-8866427 | 1.613445e-01 | 0.792 | 0 | 0 |
| Biosynthesis of DPAn-3-derived protectins and resolvins | R-HSA-9026286 | 1.613445e-01 | 0.792 | 0 | 0 |
| Regulation of IFNG signaling | R-HSA-877312 | 1.613445e-01 | 0.792 | 0 | 0 |
| Interleukin-35 Signalling | R-HSA-8984722 | 1.613445e-01 | 0.792 | 0 | 0 |
| Downregulation of ERBB2:ERBB3 signaling | R-HSA-1358803 | 1.613445e-01 | 0.792 | 0 | 0 |
| Regulation of beta-cell development | R-HSA-186712 | 1.683734e-01 | 0.774 | 0 | 0 |
| Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) | R-HSA-9661069 | 1.705217e-01 | 0.768 | 0 | 0 |
| Interleukin-6 signaling | R-HSA-1059683 | 1.705217e-01 | 0.768 | 0 | 0 |
| CD28 dependent Vav1 pathway | R-HSA-389359 | 1.705217e-01 | 0.768 | 0 | 0 |
| IL-6-type cytokine receptor ligand interactions | R-HSA-6788467 | 1.705217e-01 | 0.768 | 0 | 0 |
| Aberrant regulation of mitotic G1/S transition in cancer due to RB1 defects | R-HSA-9659787 | 1.705217e-01 | 0.768 | 0 | 0 |
| Formation of the non-canonical BAF (ncBAF) complex | R-HSA-9933947 | 1.705217e-01 | 0.768 | 0 | 0 |
| Golgi Cisternae Pericentriolar Stack Reorganization | R-HSA-162658 | 1.705217e-01 | 0.768 | 0 | 0 |
| Platelet Adhesion to exposed collagen | R-HSA-75892 | 1.705217e-01 | 0.768 | 1 | 1 |
| Regulation of TP53 Activity through Association with Co-factors | R-HSA-6804759 | 1.705217e-01 | 0.768 | 0 | 0 |
| Signaling by ERBB2 | R-HSA-1227986 | 1.722613e-01 | 0.764 | 0 | 0 |
| RNA Polymerase II Transcription Termination | R-HSA-73856 | 1.761641e-01 | 0.754 | 0 | 0 |
| Transmission across Chemical Synapses | R-HSA-112315 | 1.781061e-01 | 0.749 | 0 | 0 |
| Biosynthesis of E-series 18(R)-resolvins | R-HSA-9023661 | 1.795990e-01 | 0.746 | 0 | 0 |
| Formation of the canonical BAF (cBAF) complex | R-HSA-9933937 | 1.795990e-01 | 0.746 | 0 | 0 |
| Formation of the polybromo-BAF (pBAF) complex | R-HSA-9933939 | 1.795990e-01 | 0.746 | 0 | 0 |
| Regulation of KIT signaling | R-HSA-1433559 | 1.795990e-01 | 0.746 | 1 | 1 |
| Signal regulatory protein family interactions | R-HSA-391160 | 1.795990e-01 | 0.746 | 0 | 0 |
| Transcriptional regulation by RUNX2 | R-HSA-8878166 | 1.810965e-01 | 0.742 | 0 | 0 |
| G1/S DNA Damage Checkpoints | R-HSA-69615 | 1.840108e-01 | 0.735 | 0 | 0 |
| Signaling by PTK6 | R-HSA-8848021 | 1.840108e-01 | 0.735 | 0 | 0 |
| Signaling by Non-Receptor Tyrosine Kinases | R-HSA-9006927 | 1.840108e-01 | 0.735 | 0 | 0 |
| Signaling by PDGFRA extracellular domain mutants | R-HSA-9673770 | 1.885775e-01 | 0.725 | 0 | 0 |
| Signaling by PDGFRA transmembrane, juxtamembrane and kinase domain mutants | R-HSA-9673767 | 1.885775e-01 | 0.725 | 0 | 0 |
| Erythropoietin activates RAS | R-HSA-9027284 | 1.885775e-01 | 0.725 | 1 | 1 |
| Tristetraprolin (TTP, ZFP36) binds and destabilizes mRNA | R-HSA-450513 | 1.885775e-01 | 0.725 | 0 | 0 |
| Protein methylation | R-HSA-8876725 | 1.885775e-01 | 0.725 | 0 | 0 |
| Formation of the embryonic stem cell BAF (esBAF) complex | R-HSA-9933946 | 1.885775e-01 | 0.725 | 0 | 0 |
| Other semaphorin interactions | R-HSA-416700 | 1.885775e-01 | 0.725 | 0 | 0 |
| Aberrant regulation of mitotic exit in cancer due to RB1 defects | R-HSA-9687136 | 1.974583e-01 | 0.705 | 0 | 0 |
| Entry of Influenza Virion into Host Cell via Endocytosis | R-HSA-168275 | 1.974583e-01 | 0.705 | 0 | 0 |
| SEMA3A-Plexin repulsion signaling by inhibiting Integrin adhesion | R-HSA-399955 | 1.974583e-01 | 0.705 | 0 | 0 |
| WNT5A-dependent internalization of FZD4 | R-HSA-5099900 | 1.974583e-01 | 0.705 | 0 | 0 |
| Regulation of gene expression in late stage (branching morphogenesis) pancreatic bud precursor cells | R-HSA-210744 | 1.974583e-01 | 0.705 | 0 | 0 |
| TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest | R-HSA-6804116 | 1.974583e-01 | 0.705 | 0 | 0 |
| Developmental Cell Lineages | R-HSA-9734767 | 2.022798e-01 | 0.694 | 0 | 0 |
| Sensory processing of sound by inner hair cells of the cochlea | R-HSA-9662360 | 2.038331e-01 | 0.691 | 0 | 0 |
| Regulated Necrosis | R-HSA-5218859 | 2.038331e-01 | 0.691 | 0 | 0 |
| Platelet degranulation | R-HSA-114608 | 2.060690e-01 | 0.686 | 0 | 0 |
| Defective B4GALT7 causes EDS, progeroid type | R-HSA-3560783 | 2.062424e-01 | 0.686 | 0 | 0 |
| Defective B3GALT6 causes EDSP2 and SEMDJL1 | R-HSA-4420332 | 2.062424e-01 | 0.686 | 0 | 0 |
| Fibronectin matrix formation | R-HSA-1566977 | 2.062424e-01 | 0.686 | 0 | 0 |
| Inactivation of APC/C via direct inhibition of the APC/C complex | R-HSA-141430 | 2.062424e-01 | 0.686 | 0 | 0 |
| Antigen processing: Ub, ATP-independent proteasomal degradation | R-HSA-9912633 | 2.062424e-01 | 0.686 | 0 | 0 |
| Inhibition of the proteolytic activity of APC/C required for the onset of anaphase by mitotic spindle checkpoint components | R-HSA-141405 | 2.062424e-01 | 0.686 | 0 | 0 |
| Constitutive Signaling by EGFRvIII | R-HSA-5637810 | 2.149310e-01 | 0.668 | 0 | 0 |
| Signaling by EGFRvIII in Cancer | R-HSA-5637812 | 2.149310e-01 | 0.668 | 0 | 0 |
| Defective B3GAT3 causes JDSSDHD | R-HSA-3560801 | 2.149310e-01 | 0.668 | 0 | 0 |
| Conversion from APC/C:Cdc20 to APC/C:Cdh1 in late anaphase | R-HSA-176407 | 2.149310e-01 | 0.668 | 0 | 0 |
| Biosynthesis of aspirin-triggered D-series resolvins | R-HSA-9020265 | 2.149310e-01 | 0.668 | 0 | 0 |
| Uptake and function of anthrax toxins | R-HSA-5210891 | 2.149310e-01 | 0.668 | 0 | 0 |
| Metabolism of cofactors | R-HSA-8978934 | 2.158394e-01 | 0.666 | 0 | 0 |
| trans-Golgi Network Vesicle Budding | R-HSA-199992 | 2.198563e-01 | 0.658 | 0 | 0 |
| Biosynthesis of Lipoxins (LX) | R-HSA-2142700 | 2.235249e-01 | 0.651 | 0 | 0 |
| Signaling by ERBB2 ECD mutants | R-HSA-9665348 | 2.235249e-01 | 0.651 | 0 | 0 |
| Regulation of TP53 Activity through Methylation | R-HSA-6804760 | 2.235249e-01 | 0.651 | 0 | 0 |
| Platelet sensitization by LDL | R-HSA-432142 | 2.235249e-01 | 0.651 | 0 | 0 |
| Ephrin signaling | R-HSA-3928664 | 2.235249e-01 | 0.651 | 0 | 0 |
| Transport of Mature mRNA derived from an Intron-Containing Transcript | R-HSA-159236 | 2.238795e-01 | 0.650 | 0 | 0 |
| Response to elevated platelet cytosolic Ca2+ | R-HSA-76005 | 2.260043e-01 | 0.646 | 0 | 0 |
| E2F mediated regulation of DNA replication | R-HSA-113510 | 2.320254e-01 | 0.634 | 0 | 0 |
| Synthesis of 5-eicosatetraenoic acids | R-HSA-2142688 | 2.320254e-01 | 0.634 | 0 | 0 |
| The NLRP3 inflammasome | R-HSA-844456 | 2.320254e-01 | 0.634 | 0 | 0 |
| Other interleukin signaling | R-HSA-449836 | 2.320254e-01 | 0.634 | 0 | 0 |
| UCH proteinases | R-HSA-5689603 | 2.359812e-01 | 0.627 | 0 | 0 |
| Integration of energy metabolism | R-HSA-163685 | 2.375605e-01 | 0.624 | 0 | 0 |
| Formation of neuronal progenitor and neuronal BAF (npBAF and nBAF) | R-HSA-9934037 | 2.404332e-01 | 0.619 | 0 | 0 |
| Insertion of tail-anchored proteins into the endoplasmic reticulum membrane | R-HSA-9609523 | 2.404332e-01 | 0.619 | 0 | 0 |
| Sema4D induced cell migration and growth-cone collapse | R-HSA-416572 | 2.404332e-01 | 0.619 | 0 | 0 |
| Nephrin family interactions | R-HSA-373753 | 2.404332e-01 | 0.619 | 0 | 0 |
| PCP/CE pathway | R-HSA-4086400 | 2.440698e-01 | 0.612 | 0 | 0 |
| Sensory processing of sound | R-HSA-9659379 | 2.481187e-01 | 0.605 | 0 | 0 |
| Signaling by Ligand-Responsive EGFR Variants in Cancer | R-HSA-5637815 | 2.487496e-01 | 0.604 | 0 | 0 |
| Constitutive Signaling by Ligand-Responsive EGFR Cancer Variants | R-HSA-1236382 | 2.487496e-01 | 0.604 | 0 | 0 |
| APC-Cdc20 mediated degradation of Nek2A | R-HSA-179409 | 2.487496e-01 | 0.604 | 0 | 0 |
| Signalling to RAS | R-HSA-167044 | 2.487496e-01 | 0.604 | 0 | 0 |
| Biosynthesis of E-series 18(S)-resolvins | R-HSA-9018896 | 2.487496e-01 | 0.604 | 0 | 0 |
| Basigin interactions | R-HSA-210991 | 2.487496e-01 | 0.604 | 0 | 0 |
| Signaling by PDGFR in disease | R-HSA-9671555 | 2.569754e-01 | 0.590 | 0 | 0 |
| Attachment and Entry | R-HSA-9694614 | 2.569754e-01 | 0.590 | 0 | 0 |
| Listeria monocytogenes entry into host cells | R-HSA-8876384 | 2.569754e-01 | 0.590 | 0 | 0 |
| Transport of Mature Transcript to Cytoplasm | R-HSA-72202 | 2.602769e-01 | 0.585 | 0 | 0 |
| Notch-HLH transcription pathway | R-HSA-350054 | 2.651116e-01 | 0.577 | 0 | 0 |
| Biosynthesis of D-series resolvins | R-HSA-9018676 | 2.651116e-01 | 0.577 | 0 | 0 |
| mTORC1-mediated signalling | R-HSA-166208 | 2.651116e-01 | 0.577 | 0 | 0 |
| LDL clearance | R-HSA-8964038 | 2.651116e-01 | 0.577 | 0 | 0 |
| Interleukin-20 family signaling | R-HSA-8854691 | 2.731592e-01 | 0.564 | 0 | 0 |
| Estrogen-dependent nuclear events downstream of ESR-membrane signaling | R-HSA-9634638 | 2.731592e-01 | 0.564 | 0 | 0 |
| Interleukin receptor SHC signaling | R-HSA-912526 | 2.731592e-01 | 0.564 | 0 | 0 |
| Formation of the ureteric bud | R-HSA-9830674 | 2.731592e-01 | 0.564 | 0 | 0 |
| Carnitine shuttle | R-HSA-200425 | 2.731592e-01 | 0.564 | 0 | 0 |
| Biosynthesis of maresins | R-HSA-9018682 | 2.731592e-01 | 0.564 | 0 | 0 |
| Growth hormone receptor signaling | R-HSA-982772 | 2.731592e-01 | 0.564 | 1 | 1 |
| The role of Nef in HIV-1 replication and disease pathogenesis | R-HSA-164952 | 2.731592e-01 | 0.564 | 0 | 0 |
| Neutrophil degranulation | R-HSA-6798695 | 2.740862e-01 | 0.562 | 0 | 0 |
| RAB GEFs exchange GTP for GDP on RABs | R-HSA-8876198 | 2.764960e-01 | 0.558 | 0 | 0 |
| Interleukin-6 family signaling | R-HSA-6783589 | 2.811192e-01 | 0.551 | 0 | 0 |
| Signaling by ERBB2 TMD/JMD mutants | R-HSA-9665686 | 2.811192e-01 | 0.551 | 0 | 0 |
| Mitochondrial RNA degradation | R-HSA-9836573 | 2.811192e-01 | 0.551 | 0 | 0 |
| MITF-M-dependent gene expression | R-HSA-9856651 | 2.816710e-01 | 0.550 | 0 | 0 |
| Peptide chain elongation | R-HSA-156902 | 2.886496e-01 | 0.540 | 0 | 0 |
| Laminin interactions | R-HSA-3000157 | 2.889925e-01 | 0.539 | 0 | 0 |
| ATP-dependent chromatin remodelers | R-HSA-9932444 | 2.889925e-01 | 0.539 | 0 | 0 |
| SWI/SNF chromatin remodelers | R-HSA-9932451 | 2.889925e-01 | 0.539 | 0 | 0 |
| Biosynthesis of electrophilic ω-3 PUFA oxo-derivatives | R-HSA-9027604 | 2.889925e-01 | 0.539 | 0 | 0 |
| Sema4D in semaphorin signaling | R-HSA-400685 | 2.889925e-01 | 0.539 | 0 | 0 |
| PIWI-interacting RNA (piRNA) biogenesis | R-HSA-5601884 | 2.889925e-01 | 0.539 | 0 | 0 |
| Downstream TCR signaling | R-HSA-202424 | 2.967401e-01 | 0.528 | 0 | 0 |
| Signaling by EGFR in Cancer | R-HSA-1643713 | 2.967801e-01 | 0.528 | 0 | 0 |
| MET activates PTK2 signaling | R-HSA-8874081 | 2.967801e-01 | 0.528 | 0 | 0 |
| Bacterial Infection Pathways | R-HSA-9824439 | 2.989952e-01 | 0.524 | 0 | 0 |
| Phosphorylation of CD3 and TCR zeta chains | R-HSA-202427 | 3.044829e-01 | 0.516 | 0 | 0 |
| Biosynthesis of DPAn-3 SPMs | R-HSA-9025094 | 3.044829e-01 | 0.516 | 0 | 0 |
| Synthesis of active ubiquitin: roles of E1 and E2 enzymes | R-HSA-8866652 | 3.044829e-01 | 0.516 | 0 | 0 |
| Insulin receptor recycling | R-HSA-77387 | 3.121017e-01 | 0.506 | 0 | 0 |
| Telomere Extension By Telomerase | R-HSA-171319 | 3.121017e-01 | 0.506 | 0 | 0 |
| Inflammasomes | R-HSA-622312 | 3.121017e-01 | 0.506 | 0 | 0 |
| Iron assimilation using enterobactin | R-HSA-9638334 | 3.121017e-01 | 0.506 | 0 | 0 |
| FCGR activation | R-HSA-2029481 | 3.128775e-01 | 0.505 | 1 | 1 |
| Mitochondrial protein degradation | R-HSA-9837999 | 3.169004e-01 | 0.499 | 0 | 0 |
| Regulation of CDH11 Expression and Function | R-HSA-9759475 | 3.196376e-01 | 0.495 | 0 | 0 |
| Signaling by ERBB2 KD Mutants | R-HSA-9664565 | 3.196376e-01 | 0.495 | 0 | 0 |
| Biosynthesis of EPA-derived SPMs | R-HSA-9018679 | 3.196376e-01 | 0.495 | 0 | 0 |
| Signaling by Erythropoietin | R-HSA-9006335 | 3.196376e-01 | 0.495 | 1 | 1 |
| Regulation of gene expression in beta cells | R-HSA-210745 | 3.196376e-01 | 0.495 | 0 | 0 |
| DARPP-32 events | R-HSA-180024 | 3.196376e-01 | 0.495 | 0 | 0 |
| DDX58/IFIH1-mediated induction of interferon-alpha/beta | R-HSA-168928 | 3.209180e-01 | 0.494 | 0 | 0 |
| Ribosome Quality Control (RQC) complex extracts and degrades nascent peptide | R-HSA-9954709 | 3.249300e-01 | 0.488 | 0 | 0 |
| Energy dependent regulation of mTOR by LKB1-AMPK | R-HSA-380972 | 3.270913e-01 | 0.485 | 0 | 0 |
| Activation of the pre-replicative complex | R-HSA-68962 | 3.270913e-01 | 0.485 | 0 | 0 |
| Signaling by ERBB2 in Cancer | R-HSA-1227990 | 3.270913e-01 | 0.485 | 0 | 0 |
| NOTCH3 Intracellular Domain Regulates Transcription | R-HSA-9013508 | 3.270913e-01 | 0.485 | 0 | 0 |
| CLEC7A (Dectin-1) signaling | R-HSA-5607764 | 3.289359e-01 | 0.483 | 0 | 0 |
| Transcriptional regulation by RUNX3 | R-HSA-8878159 | 3.329354e-01 | 0.478 | 0 | 0 |
| Signaling by TGF-beta Receptor Complex | R-HSA-170834 | 3.329354e-01 | 0.478 | 0 | 0 |
| Downstream signal transduction | R-HSA-186763 | 3.344639e-01 | 0.476 | 0 | 0 |
| Budding and maturation of HIV virion | R-HSA-162588 | 3.344639e-01 | 0.476 | 0 | 0 |
| Regulation of activated PAK-2p34 by proteasome mediated degradation | R-HSA-211733 | 3.344639e-01 | 0.476 | 0 | 0 |
| Biosynthesis of DPA-derived SPMs | R-HSA-9018683 | 3.344639e-01 | 0.476 | 0 | 0 |
| Molecules associated with elastic fibres | R-HSA-2129379 | 3.344639e-01 | 0.476 | 0 | 0 |
| Evasion by RSV of host interferon responses | R-HSA-9833109 | 3.344639e-01 | 0.476 | 0 | 0 |
| Regulation of ornithine decarboxylase (ODC) | R-HSA-350562 | 3.417561e-01 | 0.466 | 0 | 0 |
| HS-GAG degradation | R-HSA-2024096 | 3.417561e-01 | 0.466 | 0 | 0 |
| Downregulation of SMAD2/3:SMAD4 transcriptional activity | R-HSA-2173795 | 3.417561e-01 | 0.466 | 0 | 0 |
| Glycolysis | R-HSA-70171 | 3.448924e-01 | 0.462 | 0 | 0 |
| Regulation of Expression and Function of Type II Classical Cadherins | R-HSA-9764260 | 3.489689e-01 | 0.457 | 0 | 0 |
| Activation of ATR in response to replication stress | R-HSA-176187 | 3.489689e-01 | 0.457 | 0 | 0 |
| Regulation of TP53 Activity through Acetylation | R-HSA-6804758 | 3.489689e-01 | 0.457 | 0 | 0 |
| Vpu mediated degradation of CD4 | R-HSA-180534 | 3.561031e-01 | 0.448 | 0 | 0 |
| DNA Damage Recognition in GG-NER | R-HSA-5696394 | 3.561031e-01 | 0.448 | 0 | 0 |
| Response of endothelial cells to shear stress | R-HSA-9860931 | 3.607261e-01 | 0.443 | 0 | 0 |
| Glycosaminoglycan-protein linkage region biosynthesis | R-HSA-1971475 | 3.631595e-01 | 0.440 | 0 | 0 |
| SARS-CoV-1 modulates host translation machinery | R-HSA-9735869 | 3.631595e-01 | 0.440 | 0 | 0 |
| Autodegradation of the E3 ubiquitin ligase COP1 | R-HSA-349425 | 3.631595e-01 | 0.440 | 0 | 0 |
| Ubiquitin-dependent degradation of Cyclin D | R-HSA-75815 | 3.631595e-01 | 0.440 | 0 | 0 |
| Nuclear Pore Complex (NPC) Disassembly | R-HSA-3301854 | 3.701391e-01 | 0.432 | 0 | 0 |
| Turbulent (oscillatory, disturbed) flow shear stress activates signaling by PIEZO1 and integrins in endothelial cells | R-HSA-9860927 | 3.701391e-01 | 0.432 | 0 | 0 |
| FBXL7 down-regulates AURKA during mitotic entry and in early mitosis | R-HSA-8854050 | 3.701391e-01 | 0.432 | 0 | 0 |
| SCF-beta-TrCP mediated degradation of Emi1 | R-HSA-174113 | 3.701391e-01 | 0.432 | 0 | 0 |
| Regulation of Apoptosis | R-HSA-169911 | 3.701391e-01 | 0.432 | 0 | 0 |
| Metabolism of ingested SeMet, Sec, MeSec into H2Se | R-HSA-2408508 | 3.701391e-01 | 0.432 | 0 | 0 |
| Influenza Infection | R-HSA-168255 | 3.712329e-01 | 0.430 | 0 | 0 |
| HS-GAG biosynthesis | R-HSA-2022928 | 3.770425e-01 | 0.424 | 0 | 0 |
| Vif-mediated degradation of APOBEC3G | R-HSA-180585 | 3.770425e-01 | 0.424 | 0 | 0 |
| AUF1 (hnRNP D0) binds and destabilizes mRNA | R-HSA-450408 | 3.770425e-01 | 0.424 | 0 | 0 |
| Degradation of DVL | R-HSA-4641258 | 3.838708e-01 | 0.416 | 0 | 0 |
| Degradation of AXIN | R-HSA-4641257 | 3.838708e-01 | 0.416 | 0 | 0 |
| GSK3B and BTRC:CUL1-mediated-degradation of NFE2L2 | R-HSA-9762114 | 3.838708e-01 | 0.416 | 0 | 0 |
| Ovarian tumor domain proteases | R-HSA-5689896 | 3.838708e-01 | 0.416 | 0 | 0 |
| Elastic fibre formation | R-HSA-1566948 | 3.906246e-01 | 0.408 | 0 | 0 |
| MET promotes cell motility | R-HSA-8875878 | 3.906246e-01 | 0.408 | 0 | 0 |
| Differentiation of Keratinocytes in Interfollicular Epidermis in Mammalian Skin | R-HSA-9725554 | 3.973048e-01 | 0.401 | 0 | 0 |
| Cross-presentation of soluble exogenous antigens (endosomes) | R-HSA-1236978 | 3.973048e-01 | 0.401 | 0 | 0 |
| GSK3B-mediated proteasomal degradation of PD-L1(CD274) | R-HSA-9929356 | 3.973048e-01 | 0.401 | 0 | 0 |
| Plasma lipoprotein clearance | R-HSA-8964043 | 3.973048e-01 | 0.401 | 0 | 0 |
| Stabilization of p53 | R-HSA-69541 | 3.973048e-01 | 0.401 | 0 | 0 |
| Pentose phosphate pathway | R-HSA-71336 | 3.973048e-01 | 0.401 | 0 | 0 |
| Signaling by ALK | R-HSA-201556 | 3.973048e-01 | 0.401 | 0 | 0 |
| Cellular responses to mechanical stimuli | R-HSA-9855142 | 4.034874e-01 | 0.394 | 0 | 0 |
| Regulation of RUNX3 expression and activity | R-HSA-8941858 | 4.039121e-01 | 0.394 | 0 | 0 |
| Hh mutants are degraded by ERAD | R-HSA-5362768 | 4.104475e-01 | 0.387 | 0 | 0 |
| NIK-->noncanonical NF-kB signaling | R-HSA-5676590 | 4.104475e-01 | 0.387 | 0 | 0 |
| Transcriptional Regulation by VENTX | R-HSA-8853884 | 4.104475e-01 | 0.387 | 0 | 0 |
| PKMTs methylate histone lysines | R-HSA-3214841 | 4.104475e-01 | 0.387 | 0 | 0 |
| Interferon alpha/beta signaling | R-HSA-909733 | 4.149198e-01 | 0.382 | 0 | 0 |
| Role of phospholipids in phagocytosis | R-HSA-2029485 | 4.149198e-01 | 0.382 | 0 | 0 |
| Degradation of CRY and PER proteins | R-HSA-9932298 | 4.169116e-01 | 0.380 | 0 | 0 |
| Degradation of GLI1 by the proteasome | R-HSA-5610780 | 4.169116e-01 | 0.380 | 0 | 0 |
| Degradation of GLI2 by the proteasome | R-HSA-5610783 | 4.169116e-01 | 0.380 | 0 | 0 |
| GLI3 is processed to GLI3R by the proteasome | R-HSA-5610785 | 4.169116e-01 | 0.380 | 0 | 0 |
| Glucose metabolism | R-HSA-70326 | 4.224810e-01 | 0.374 | 0 | 0 |
| Rab regulation of trafficking | R-HSA-9007101 | 4.224810e-01 | 0.374 | 0 | 0 |
| Hh mutants abrogate ligand secretion | R-HSA-5387390 | 4.296291e-01 | 0.367 | 0 | 0 |
| TGF-beta receptor signaling activates SMADs | R-HSA-2173789 | 4.296291e-01 | 0.367 | 0 | 0 |
| Response of Mtb to phagocytosis | R-HSA-9637690 | 4.296291e-01 | 0.367 | 0 | 0 |
| RMTs methylate histone arginines | R-HSA-3214858 | 4.358840e-01 | 0.361 | 0 | 0 |
| Synthesis of Leukotrienes (LT) and Eoxins (EX) | R-HSA-2142691 | 4.358840e-01 | 0.361 | 0 | 0 |
| Methylation | R-HSA-156581 | 4.358840e-01 | 0.361 | 0 | 0 |
| Cyclin D associated events in G1 | R-HSA-69231 | 4.358840e-01 | 0.361 | 1 | 1 |
| G1 Phase | R-HSA-69236 | 4.358840e-01 | 0.361 | 1 | 0 |
| Diseases associated with glycosaminoglycan metabolism | R-HSA-3560782 | 4.420707e-01 | 0.355 | 0 | 0 |
| Regulation of MITF-M-dependent genes involved in pigmentation | R-HSA-9824585 | 4.420707e-01 | 0.355 | 0 | 0 |
| Asymmetric localization of PCP proteins | R-HSA-4608870 | 4.420707e-01 | 0.355 | 0 | 0 |
| Defective CFTR causes cystic fibrosis | R-HSA-5678895 | 4.420707e-01 | 0.355 | 0 | 0 |
| Dectin-1 mediated noncanonical NF-kB signaling | R-HSA-5607761 | 4.420707e-01 | 0.355 | 0 | 0 |
| p53-Independent G1/S DNA Damage Checkpoint | R-HSA-69613 | 4.420707e-01 | 0.355 | 0 | 0 |
| Ubiquitin-Mediated Degradation of Phosphorylated Cdc25A | R-HSA-69601 | 4.420707e-01 | 0.355 | 0 | 0 |
| mRNA Splicing - Minor Pathway | R-HSA-72165 | 4.481900e-01 | 0.349 | 0 | 0 |
| Cell recruitment (pro-inflammatory response) | R-HSA-9664424 | 4.481900e-01 | 0.349 | 0 | 0 |
| Purinergic signaling in leishmaniasis infection | R-HSA-9660826 | 4.481900e-01 | 0.349 | 0 | 0 |
| Regulation of pyruvate metabolism | R-HSA-9861718 | 4.481900e-01 | 0.349 | 0 | 0 |
| Host Interactions of HIV factors | R-HSA-162909 | 4.485417e-01 | 0.348 | 0 | 0 |
| Neuronal System | R-HSA-112316 | 4.505323e-01 | 0.346 | 0 | 0 |
| FCGR3A-mediated IL10 synthesis | R-HSA-9664323 | 4.595088e-01 | 0.338 | 1 | 1 |
| GPER1 signaling | R-HSA-9634597 | 4.602290e-01 | 0.337 | 0 | 0 |
| NGF-stimulated transcription | R-HSA-9031628 | 4.602290e-01 | 0.337 | 0 | 0 |
| NOTCH1 Intracellular Domain Regulates Transcription | R-HSA-2122947 | 4.661502e-01 | 0.331 | 0 | 0 |
| Regulation of RAS by GAPs | R-HSA-5658442 | 4.720068e-01 | 0.326 | 0 | 0 |
| Complex IV assembly | R-HSA-9864848 | 4.777995e-01 | 0.321 | 0 | 0 |
| Activation of NF-kappaB in B cells | R-HSA-1169091 | 4.777995e-01 | 0.321 | 0 | 0 |
| Oxygen-dependent proline hydroxylation of Hypoxia-inducible Factor Alpha | R-HSA-1234176 | 4.777995e-01 | 0.321 | 0 | 0 |
| Hedgehog ligand biogenesis | R-HSA-5358346 | 4.777995e-01 | 0.321 | 0 | 0 |
| Drug ADME | R-HSA-9748784 | 4.867352e-01 | 0.313 | 0 | 0 |
| Golgi Associated Vesicle Biogenesis | R-HSA-432722 | 4.891960e-01 | 0.311 | 0 | 0 |
| Signaling by NOTCH3 | R-HSA-9012852 | 5.003452e-01 | 0.301 | 0 | 0 |
| Beta-catenin independent WNT signaling | R-HSA-3858494 | 5.020794e-01 | 0.299 | 0 | 0 |
| Signaling by EGFR | R-HSA-177929 | 5.058287e-01 | 0.296 | 0 | 0 |
| Transcriptional activity of SMAD2/SMAD3:SMAD4 heterotrimer | R-HSA-2173793 | 5.058287e-01 | 0.296 | 0 | 0 |
| Ribosome-associated quality control | R-HSA-9948299 | 5.089642e-01 | 0.293 | 0 | 0 |
| Dectin-2 family | R-HSA-5621480 | 5.112524e-01 | 0.291 | 1 | 1 |
| HIV Infection | R-HSA-162906 | 5.113816e-01 | 0.291 | 0 | 0 |
| Early SARS-CoV-2 Infection Events | R-HSA-9772572 | 5.166168e-01 | 0.287 | 0 | 0 |
| Innate Immune System | R-HSA-168249 | 5.215701e-01 | 0.283 | 1 | 0 |
| Heparan sulfate/heparin (HS-GAG) metabolism | R-HSA-1638091 | 5.219228e-01 | 0.282 | 0 | 0 |
| Metabolism of non-coding RNA | R-HSA-194441 | 5.219228e-01 | 0.282 | 0 | 0 |
| snRNP Assembly | R-HSA-191859 | 5.219228e-01 | 0.282 | 0 | 0 |
| Extension of Telomeres | R-HSA-180786 | 5.219228e-01 | 0.282 | 0 | 0 |
| Signaling by NOTCH1 HD+PEST Domain Mutants in Cancer | R-HSA-2894858 | 5.271708e-01 | 0.278 | 0 | 0 |
| Constitutive Signaling by NOTCH1 HD+PEST Domain Mutants | R-HSA-2894862 | 5.271708e-01 | 0.278 | 0 | 0 |
| Signaling by NOTCH1 PEST Domain Mutants in Cancer | R-HSA-2644602 | 5.271708e-01 | 0.278 | 0 | 0 |
| Constitutive Signaling by NOTCH1 PEST Domain Mutants | R-HSA-2644606 | 5.271708e-01 | 0.278 | 0 | 0 |
| Signaling by NOTCH1 in Cancer | R-HSA-2644603 | 5.271708e-01 | 0.278 | 0 | 0 |
| Metabolism of polyamines | R-HSA-351202 | 5.271708e-01 | 0.278 | 0 | 0 |
| IRS-related events triggered by IGF1R | R-HSA-2428928 | 5.323615e-01 | 0.274 | 0 | 0 |
| Regulation of RUNX2 expression and activity | R-HSA-8939902 | 5.323615e-01 | 0.274 | 0 | 0 |
| Signaling by PDGF | R-HSA-186797 | 5.374955e-01 | 0.270 | 0 | 0 |
| Mitochondrial protein import | R-HSA-1268020 | 5.374955e-01 | 0.270 | 0 | 0 |
| Cell surface interactions at the vascular wall | R-HSA-202733 | 5.380263e-01 | 0.269 | 1 | 1 |
| Asparagine N-linked glycosylation | R-HSA-446203 | 5.384723e-01 | 0.269 | 0 | 0 |
| IGF1R signaling cascade | R-HSA-2428924 | 5.475961e-01 | 0.262 | 0 | 0 |
| Insulin receptor signalling cascade | R-HSA-74751 | 5.475961e-01 | 0.262 | 0 | 0 |
| Nucleotide-binding domain, leucine rich repeat containing receptor (NLR) signaling pathways | R-HSA-168643 | 5.475961e-01 | 0.262 | 0 | 0 |
| Binding and Uptake of Ligands by Scavenger Receptors | R-HSA-2173782 | 5.521814e-01 | 0.258 | 0 | 0 |
| Translation | R-HSA-72766 | 5.524122e-01 | 0.258 | 0 | 0 |
| Signaling by Type 1 Insulin-like Growth Factor 1 Receptor (IGF1R) | R-HSA-2404192 | 5.525638e-01 | 0.258 | 0 | 0 |
| Cellular response to hypoxia | R-HSA-1234174 | 5.525638e-01 | 0.258 | 0 | 0 |
| Regulation of expression of SLITs and ROBOs | R-HSA-9010553 | 5.585897e-01 | 0.253 | 0 | 0 |
| Protein localization | R-HSA-9609507 | 5.617695e-01 | 0.250 | 0 | 0 |
| Kidney development | R-HSA-9830369 | 5.623371e-01 | 0.250 | 0 | 0 |
| Influenza Viral RNA Transcription and Replication | R-HSA-168273 | 5.680801e-01 | 0.246 | 0 | 0 |
| Fatty acyl-CoA biosynthesis | R-HSA-75105 | 5.766004e-01 | 0.239 | 0 | 0 |
| Downstream signaling events of B Cell Receptor (BCR) | R-HSA-1168372 | 5.766004e-01 | 0.239 | 0 | 0 |
| Degradation of beta-catenin by the destruction complex | R-HSA-195253 | 5.766004e-01 | 0.239 | 0 | 0 |
| ECM proteoglycans | R-HSA-3000178 | 5.812514e-01 | 0.236 | 0 | 0 |
| Retinoid metabolism and transport | R-HSA-975634 | 5.812514e-01 | 0.236 | 0 | 0 |
| Hedgehog 'on' state | R-HSA-5632684 | 5.812514e-01 | 0.236 | 0 | 0 |
| Metal ion assimilation from the host | R-HSA-9638482 | 5.812514e-01 | 0.236 | 0 | 0 |
| Signaling by TGFB family members | R-HSA-9006936 | 5.835704e-01 | 0.234 | 0 | 0 |
| Interconversion of nucleotide di- and triphosphates | R-HSA-499943 | 5.858516e-01 | 0.232 | 0 | 0 |
| Nuclear Events (kinase and transcription factor activation) | R-HSA-198725 | 5.858516e-01 | 0.232 | 0 | 0 |
| Selenoamino acid metabolism | R-HSA-2408522 | 5.956673e-01 | 0.225 | 0 | 0 |
| ISG15 antiviral mechanism | R-HSA-1169408 | 5.993527e-01 | 0.222 | 0 | 0 |
| Signaling by NOTCH1 | R-HSA-1980143 | 6.037551e-01 | 0.219 | 0 | 0 |
| Integrin cell surface interactions | R-HSA-216083 | 6.124161e-01 | 0.213 | 0 | 0 |
| Interleukin-10 signaling | R-HSA-6783783 | 6.124161e-01 | 0.213 | 0 | 0 |
| ABC transporter disorders | R-HSA-5619084 | 6.124161e-01 | 0.213 | 0 | 0 |
| Developmental Lineage of Pancreatic Acinar Cells | R-HSA-9925561 | 6.166757e-01 | 0.210 | 0 | 0 |
| Metabolic disorders of biological oxidation enzymes | R-HSA-5579029 | 6.166757e-01 | 0.210 | 0 | 0 |
| C-type lectin receptors (CLRs) | R-HSA-5621481 | 6.190719e-01 | 0.208 | 1 | 0 |
| High laminar flow shear stress activates signaling by PIEZO1 and PECAM1:CDH5:KDR in endothelial cells | R-HSA-9856530 | 6.208888e-01 | 0.207 | 0 | 0 |
| Signaling by MET | R-HSA-6806834 | 6.208888e-01 | 0.207 | 0 | 0 |
| Leishmania parasite growth and survival | R-HSA-9664433 | 6.247589e-01 | 0.204 | 1 | 0 |
| Anti-inflammatory response favouring Leishmania parasite infection | R-HSA-9662851 | 6.247589e-01 | 0.204 | 1 | 0 |
| Biosynthesis of DHA-derived SPMs | R-HSA-9018677 | 6.250559e-01 | 0.204 | 0 | 0 |
| Metabolism of fat-soluble vitamins | R-HSA-6806667 | 6.250559e-01 | 0.204 | 0 | 0 |
| Cytoprotection by HMOX1 | R-HSA-9707564 | 6.332538e-01 | 0.198 | 0 | 0 |
| TNFR2 non-canonical NF-kB pathway | R-HSA-5668541 | 6.332538e-01 | 0.198 | 0 | 0 |
| Global Genome Nucleotide Excision Repair (GG-NER) | R-HSA-5696399 | 6.372857e-01 | 0.196 | 0 | 0 |
| Sulfur amino acid metabolism | R-HSA-1614635 | 6.491189e-01 | 0.188 | 0 | 0 |
| Pyruvate metabolism | R-HSA-70268 | 6.529773e-01 | 0.185 | 0 | 0 |
| ER-Phagosome pathway | R-HSA-1236974 | 6.605680e-01 | 0.180 | 0 | 0 |
| PELO:HBS1L and ABCE1 dissociate a ribosome on a non-stop mRNA | R-HSA-9954714 | 6.679937e-01 | 0.175 | 0 | 0 |
| Nonsense Mediated Decay (NMD) independent of the Exon Junction Complex (EJC) | R-HSA-975956 | 6.716457e-01 | 0.173 | 0 | 0 |
| Signaling by Insulin receptor | R-HSA-74752 | 6.752577e-01 | 0.171 | 0 | 0 |
| Plasma lipoprotein assembly, remodeling, and clearance | R-HSA-174824 | 6.752577e-01 | 0.171 | 0 | 0 |
| ZNF598 and the Ribosome-associated Quality Trigger (RQT) complex dissociate a ribosome stalled on a no-go mRNA | R-HSA-9954716 | 6.858586e-01 | 0.164 | 0 | 0 |
| Mitochondrial Fatty Acid Beta-Oxidation | R-HSA-77289 | 6.858586e-01 | 0.164 | 0 | 0 |
| Eukaryotic Translation Termination | R-HSA-72764 | 6.893151e-01 | 0.162 | 0 | 0 |
| Formation of a pool of free 40S subunits | R-HSA-72689 | 6.893151e-01 | 0.162 | 0 | 0 |
| Role of LAT2/NTAL/LAB on calcium mobilization | R-HSA-2730905 | 6.927339e-01 | 0.159 | 1 | 1 |
| Fatty acid metabolism | R-HSA-8978868 | 6.946262e-01 | 0.158 | 0 | 0 |
| Post-translational protein phosphorylation | R-HSA-8957275 | 6.994596e-01 | 0.155 | 0 | 0 |
| Signaling by ROBO receptors | R-HSA-376176 | 7.023260e-01 | 0.153 | 0 | 0 |
| Glycerophospholipid biosynthesis | R-HSA-1483206 | 7.023260e-01 | 0.153 | 0 | 0 |
| Mitotic Spindle Checkpoint | R-HSA-69618 | 7.060389e-01 | 0.151 | 0 | 0 |
| ABC-family proteins mediated transport | R-HSA-382556 | 7.060389e-01 | 0.151 | 0 | 0 |
| Selenocysteine synthesis | R-HSA-2408557 | 7.092746e-01 | 0.149 | 0 | 0 |
| Interleukin-1 signaling | R-HSA-9020702 | 7.092746e-01 | 0.149 | 0 | 0 |
| Viral mRNA Translation | R-HSA-192823 | 7.156402e-01 | 0.145 | 0 | 0 |
| Response of EIF2AK4 (GCN2) to amino acid deficiency | R-HSA-9633012 | 7.187708e-01 | 0.143 | 0 | 0 |
| Cargo recognition for clathrin-mediated endocytosis | R-HSA-8856825 | 7.187708e-01 | 0.143 | 0 | 0 |
| Opioid Signalling | R-HSA-111885 | 7.187708e-01 | 0.143 | 0 | 0 |
| Nucleotide Excision Repair | R-HSA-5696398 | 7.249297e-01 | 0.140 | 0 | 0 |
| Platelet homeostasis | R-HSA-418346 | 7.279586e-01 | 0.138 | 0 | 0 |
| SRP-dependent cotranslational protein targeting to membrane | R-HSA-1799339 | 7.309543e-01 | 0.136 | 0 | 0 |
| GTP hydrolysis and joining of the 60S ribosomal subunit | R-HSA-72706 | 7.339173e-01 | 0.134 | 0 | 0 |
| L13a-mediated translational silencing of Ceruloplasmin expression | R-HSA-156827 | 7.339173e-01 | 0.134 | 0 | 0 |
| Antigen processing-Cross presentation | R-HSA-1236975 | 7.339173e-01 | 0.134 | 0 | 0 |
| Nonsense-Mediated Decay (NMD) | R-HSA-927802 | 7.454481e-01 | 0.128 | 0 | 0 |
| Nonsense Mediated Decay (NMD) enhanced by the Exon Junction Complex (EJC) | R-HSA-975957 | 7.454481e-01 | 0.128 | 0 | 0 |
| Regulation of Insulin-like Growth Factor (IGF) transport and uptake by Insulin-like Growth Factor Binding Proteins (IGFBPs) | R-HSA-381426 | 7.537689e-01 | 0.123 | 0 | 0 |
| Immunoregulatory interactions between a Lymphoid and a non-Lymphoid cell | R-HSA-198933 | 7.603605e-01 | 0.119 | 0 | 0 |
| Eukaryotic Translation Initiation | R-HSA-72613 | 7.618192e-01 | 0.118 | 0 | 0 |
| Cap-dependent Translation Initiation | R-HSA-72737 | 7.618192e-01 | 0.118 | 0 | 0 |
| Mitochondrial biogenesis | R-HSA-1592230 | 7.644441e-01 | 0.117 | 0 | 0 |
| Metabolism of carbohydrates and carbohydrate derivatives | R-HSA-71387 | 7.703141e-01 | 0.113 | 0 | 0 |
| Infection with Mycobacterium tuberculosis | R-HSA-9635486 | 7.746589e-01 | 0.111 | 0 | 0 |
| GPCR downstream signalling | R-HSA-388396 | 7.752054e-01 | 0.111 | 0 | 0 |
| Metabolism of vitamins and cofactors | R-HSA-196854 | 7.959975e-01 | 0.099 | 0 | 0 |
| Late Phase of HIV Life Cycle | R-HSA-162599 | 8.292362e-01 | 0.081 | 0 | 0 |
| Biosynthesis of specialized proresolving mediators (SPMs) | R-HSA-9018678 | 8.311216e-01 | 0.080 | 0 | 0 |
| FCERI mediated NF-kB activation | R-HSA-2871837 | 8.329863e-01 | 0.079 | 1 | 1 |
| Visual phototransduction | R-HSA-2187338 | 8.384585e-01 | 0.077 | 0 | 0 |
| Phase I - Functionalization of compounds | R-HSA-211945 | 8.410196e-01 | 0.075 | 0 | 0 |
| Antigen processing: Ubiquitination & Proteasome degradation | R-HSA-983168 | 8.463850e-01 | 0.072 | 0 | 0 |
| Developmental Cell Lineages of the Exocrine Pancreas | R-HSA-9820448 | 8.471853e-01 | 0.072 | 0 | 0 |
| Arachidonate metabolism | R-HSA-2142753 | 8.471853e-01 | 0.072 | 0 | 0 |
| Signaling by GPCR | R-HSA-372790 | 8.535814e-01 | 0.069 | 0 | 0 |
| HIV Life Cycle | R-HSA-162587 | 8.554433e-01 | 0.068 | 0 | 0 |
| Cellular response to starvation | R-HSA-9711097 | 8.570408e-01 | 0.067 | 0 | 0 |
| Interferon gamma signaling | R-HSA-877300 | 8.586208e-01 | 0.066 | 0 | 0 |
| Phospholipid metabolism | R-HSA-1483257 | 8.627104e-01 | 0.064 | 0 | 0 |
| Major pathway of rRNA processing in the nucleolus and cytosol | R-HSA-6791226 | 8.762790e-01 | 0.057 | 0 | 0 |
| G alpha (s) signalling events | R-HSA-418555 | 8.776475e-01 | 0.057 | 0 | 0 |
| Respiratory electron transport | R-HSA-611105 | 8.868145e-01 | 0.052 | 0 | 0 |
| Diseases of glycosylation | R-HSA-3781865 | 8.941262e-01 | 0.049 | 0 | 0 |
| rRNA processing in the nucleus and cytosol | R-HSA-8868773 | 8.987377e-01 | 0.046 | 0 | 0 |
| Glycosaminoglycan metabolism | R-HSA-1630316 | 9.042222e-01 | 0.044 | 0 | 0 |
| Aerobic respiration and respiratory electron transport | R-HSA-1428517 | 9.085535e-01 | 0.042 | 0 | 0 |
| Infection with Enterobacteria | R-HSA-9640148 | 9.143206e-01 | 0.039 | 0 | 0 |
| Neddylation | R-HSA-8951664 | 9.306807e-01 | 0.031 | 0 | 0 |
| Class I MHC mediated antigen processing & presentation | R-HSA-983169 | 9.381244e-01 | 0.028 | 0 | 0 |
| rRNA processing | R-HSA-72312 | 9.386905e-01 | 0.027 | 0 | 0 |
| Biological oxidations | R-HSA-211859 | 9.401524e-01 | 0.027 | 0 | 0 |
| Metabolism of nucleotides | R-HSA-15869 | 9.413691e-01 | 0.026 | 0 | 0 |
| Phase II - Conjugation of compounds | R-HSA-156580 | 9.433013e-01 | 0.025 | 0 | 0 |
| Disorders of transmembrane transporters | R-HSA-5619115 | 9.481499e-01 | 0.023 | 0 | 0 |
| Diseases of metabolism | R-HSA-5668914 | 9.588909e-01 | 0.018 | 0 | 0 |
| Metabolism of amino acids and derivatives | R-HSA-71291 | 9.730592e-01 | 0.012 | 0 | 0 |
| G alpha (i) signalling events | R-HSA-418594 | 9.915036e-01 | 0.004 | 0 | 0 |
| Metabolism of lipids | R-HSA-556833 | 9.994027e-01 | 0.000 | 0 | 0 |
| Transport of small molecules | R-HSA-382551 | 9.998532e-01 | 0.000 | 0 | 0 |
| Sensory Perception | R-HSA-9709957 | 9.999286e-01 | 0.000 | 0 | 0 |
| Metabolism | R-HSA-1430728 | 9.999659e-01 | 0.000 | 0 | 0 |
| CD209 (DC-SIGN) signaling | R-HSA-5621575 | 1.000000e+00 | 0.000 | 1 | 1 |
| Erythropoietin activates Phosphoinositide-3-kinase (PI3K) | R-HSA-9027276 | 1.000000e+00 | 0.000 | 1 | 1 |
| Erythropoietin activates Phospholipase C gamma (PLCG) | R-HSA-9027277 | 1.000000e+00 | 0.000 | 1 | 1 |
| Erythropoietin activates STAT5 | R-HSA-9027283 | 1.000000e+00 | 0.000 | 1 | 1 |
| Signaling by KIT in disease | R-HSA-9669938 | 1.000000e+00 | 0.000 | 1 | 0 |
| Signaling by phosphorylated juxtamembrane, extracellular and kinase domain KIT mutants | R-HSA-9670439 | 1.000000e+00 | 0.000 | 1 | 1 |
| Signaling by CSF1 (M-CSF) in myeloid cells | R-HSA-9680350 | 1.000000e+00 | 0.000 | 1 | 1 |
Top15 pathways (red highlights are reference pathways)
Compared with reference pathways
